# Food and Drug Administration Modernization Act of 1997: Modifications to the List of Recognized Standards, Recognition List Number: 028 > Briefs, arguments, decisions, and more. URL: https://www.frixlaw.com/law-library/documents/fr%3A2012-6389 ## Record - **Collection:** Federal Register - **Document type:** Notice - **Published:** March 16, 2012 - **Citation:** 77 FR 15765 ## Text DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA-2004-N-0451] Food and Drug Administration Modernization Act of 1997: Modifications to the List of Recognized Standards, Recognition List Number: 028 AGENCY: Food and Drug Administration, HHS. ACTION: Notice. SUMMARY: The Food and Drug Administration (FDA) is announcing a publication containing modifications the Agency is making to the list of standards FDA recognizes for use in premarket reviews (FDA recognized consensus standards). This publication, entitled “Modifications to the List of Recognized Standards, Recognition List Number: 028” (Recognition List Number: 028), will assist manufacturers who elect to declare conformity with consensus standards to meet certain requirements for medical devices. DATES: Submit either electronic or written comments concerning this document at any time. See section VII of this document for the effective date of the recognition of standards announced in this document. ADDRESSES: Submit written requests for single copies of “Modifications to the List of Recognized Standards, Recognition List Number: 028” to the Division of Small Manufacturers, International and Consumer Assistance, Center for Devices and Radiological Health, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 66, Silver Spring, MD 20993. Send two self-addressed adhesive labels to assist that office in processing your requests, or fax your request to 301-847-8149. Submit electronic comments concerning this document to standards@cdrh.fda.gov. Submit written comments concerning this document, or recommendations for additional standards for recognition, to the contact person (see FOR FURTHER INFORMATION CONTACT ). This document may also be accessed on FDA's Internet site at http://www.fda.gov/MedicalDevices/DeviceRegulationandGuidance/Standards/ucm123792.htm . See section VI of this document for electronic access to the searchable database for the current list of FDA recognized consensus standards, including Recognition List Number: 028 modifications and other standards related information. FOR FURTHER INFORMATION CONTACT: Scott A. Colburn, Center for Devices and Radiological Health, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 66, Rm. 3628, Silver Spring, MD 20993, 301-796-6574. I. Background Section 204 of the Food and Drug Administration Modernization Act of 1997 (FDAMA) (Pub. L. 105-115) amended section 514 of the Federal Food, Drug, and Cosmetic Act (the FD&C Act) (21 U.S.C. 360d). Amended section 514 allows FDA to recognize consensus standards developed by international and national organizations for use in satisfying portions of device premarket review submissions or other requirements. In a notice published in the Federal Register of February 25, 1998 (63 FR 9561), FDA announced the availability of a guidance entitled “Recognition and Use of Consensus Standards.” The notice described how FDA would implement its standard recognition program and provided the initial list of recognized standards. Modifications to the initial list of recognized standards, as published in the Federal Register, are identified in table 1 of this document. Table 1—Previous Publication of Standard Recognition Lists February 25, 1998 (63 FR 9561) October 16, 1998 (63 FR 55617) July 12, 1999 (64 FR 37546) November 15, 2000 (65 FR 69022) May 7, 2001 (66 FR 23032) January 14, 2002 (67 FR 1774) October 2, 2002 (67 FR 61893) April 28, 2003 (68 FR 22391) March 8, 2004 (69 FR 10712) June 18, 2004 (69 FR 34176) October 4, 2004 (69 FR 59240) May 27, 2005 (70 FR 30756) November 8, 2005 (70 FR 67713) March 31, 2006 (71 FR 16313) June 23, 2006 (71 FR 36121) November 3, 2006 (71 FR 64718) May 21, 2007 (72 FR 28500) September 12, 2007 (72 FR 52142) December 19, 2007 (72 FR 71924) September 9, 2008 (73 FR 52358) March, 18, 2009 (74 FR 11586) September 8, 2009 (74 FR 46203) May 5, 2010 (75 FR 24711) June 10, 2010 (75 FR 32943) October 4, 2010 (75 FR 61148) March 14, 2011 (76 FR 13631) August 2, 2011 (76 FR 46300) These notices describe the addition, withdrawal, and revision of certain standards recognized by FDA. The Agency maintains “hypertext markup language (HTML)” and “portable document format (PDF)” versions of the list of “FDA Recognized Consensus Standards.” Both versions are publicly accessible at the Agency's Internet site. See section VI of this document for electronic access information. Interested persons should review the supplementary information sheet for the standard to understand fully the extent to which FDA recognizes the standard. II. Modifications to the List of Recognized Standards, Recognition List Number: 028 FDA is announcing the addition, withdrawal, correction, and revision of certain consensus standards the Agency will recognize for use in satisfying premarket reviews and other requirements for devices. FDA will incorporate these modifications in the list of FDA Recognized Consensus Standards in the Agency's searchable database. FDA will use the term “Recognition List Number: 028” to identify these current modifications. In table 2 of this document, FDA describes the following modifications: (1) The withdrawal of standards and their replacement by others, (2) the correction of errors made by FDA in listing previously recognized standards, and (3) the changes to the supplementary information sheets of recognized standards that describe revisions to the applicability of the standards. In section III of this document, FDA lists modifications the Agency is making that involve the initial addition of standards not previously recognized by FDA. Table 2—Modifications to the List of Recognized Standards Old recognition No. Replacement recognition No. Title of standard 1 Change A. Anesthesia 1-15 ISO 5361-4 Second edition 1987-12-15 Tracheal tubes—Part 4: Cole type Contact person. 1-18 ISO 8359 Second edition 1996-12-15 Oxygen concentrators for medical use—Safety requirements Contact person. 1-35 ISO 5361 First edition 1999-09-15 Corrected and reprinted 1999-12-15 Anaesthetic and respiratory equipment—Tracheal tubes and connectors Contact person. 1-36 ISO 5366-3 Second edition 2001-08-15 Anaesthetic and respiratory equipment—Tracheostomy tubes—Part 3: Pediatric tracheostomy tubes Contact person. 1-44 ISO 5366-1 Fourth edition 2000-12-15 Anaesthetic and respiratory equipment—Tracheostomy tubes—Part 1: Tubes and connectors for use in adults Contact person. 1-46 ISO 5367 Fourth edition 2000-06-01 Breathing tubes intended for use with anaesthetic apparatus and ventilators Contact person. 1-56 CGA V-7.1:1997 (Reaffirmed 2008) Standard Method of Determining Cylinder Valve Outlet Connections for Medical Gases Contact person. 1-57 ASTM F1101-90 (Reapproved 2003) 1 Standard Specification for Ventilators Intended for Use During Anesthesia Contact person. 1-58 ASTM G175-03 (Reapproved 2011) Standard Test Method for Evaluating the Ignition Sensitivity and Fault Tolerance of Oxygen Regulators Used for Medical and Emergency Applications Reaffirmation. 1-60 IEC 60601-2-12 [ISO 10651-1] Second edition 2001-10 Medical electrical equipment—Part 2-12: Particular requirements for the safety of lung ventilators—Critical care ventilators Contact person. 1-62 ISO 5356-1 Third edition 2004-05-15 Anaesthetic and respiratory equipment—Conical connectors: Part 1: Cones and sockets Contact person. 1-69 ASTM F 1464-93 (Reapproved 2005) Standard Specification for Oxygen Concentrators for Domiciliary Use Contact person. 1-70 ASTM F 1246-91 (Reapproved 2005) Standard Specification for Electrically Powered Home Care Ventilators, Part 1—Positive-Pressure Ventilators and Ventilator Circuits Contact person. 1-72 ISO 10651-5 First edition 2006-02-01 Lung ventilators for medical use—Particular requirements for basic safety and essential performance—Part 5: Gas-powered emergency resuscitators Contact person. 1-73 ISO 10651-4 First edition 2002-03-01 Lung ventilators—Part 4: Particular requirements for operator-powered resuscitators Contact person. 1-75 ISO 5362 Fourth edition 2006-06-01 Anaesthetic reservoir bags Contact person. 1-79 ISO 26825 First edition 2008-08-15 Corrected version 2009-09-15 Anaesthetic and respiratory equipment—User-applied labels for syringes containing drugs used during anaesthesia—Colours, design and performance Contact person. B. Biocompatibility 2-87 2-174 ISO 10993-10 Third Edition 2010-08-01 Biological evaluation of medical devices—Part 10: Tests for irritation and skin sensitization Withdrawn and replaced with newer version. 2-93 ASTM F763-04 (Reapproved 2010) Standard Practice for Short-Term Screening of Implant Materials Reaffirmation. 2-94 ASTM F981-04 (Reapproved 2010) Standard Practice for Assessment of Compatibility of Biomaterials for Surgical Implants with Respect to Effect of Materials on Muscle and Bone Reaffirmation. 2-108 ASTM F1905-98 Standard Practice for Selecting Tests for Determining the Propensity of Materials to Cause Immunotoxicity Withdrawn. 2-114 ASTM F1877-05 (Reapproved 2010) Standard Practice for Characterization of Particles Reaffirmation. 2-117 ANSI/AAMI/ISO 10993-3:2003(R)2009 Biological evaluation of medical devices—Part 3: Tests for genotoxicity, carcinogenicity, and reproductive toxicity Extent of recognition and Contact person. 2-118 ANSI/AAMI/ISO 10993-11:2006/(R)2010 Biological evaluation of medical devices—Part 11: Tests for systemic toxicity Reaffirmation. 2-120 ANSI/AAMI/ISO 10993-6:2007/(R)2010 Biological evaluation of medical devices—Part 6: Tests for local effects after implantation Reaffirmation. 2-126 ASTM F748-06 (Reapproved 2010) Standard Practice for Selecting Generic Biological Test Methods for Materials and Devices Reaffirmation. 2-134 ASTM F2065-00 (Reapproved 2010) Standard Practice for Testing for Alternative Pathway Complement Activation in Serum by Solid Materials Reaffirmation. 2-155 ASTM F2147-01 (Reapproved 2010) Standard Practice for Guinea Pig: Split Adjuvant and Closed Patch Testing for Contact Allergens Reaffirmation. 2-157 2-184 USP34-NF29:2011<87> Biological Reactivity Tests, In Vitro—Direct Contact Test Withdrawn and replaced with newer version. 2-158 2-185 USP 34-NF29:2011 Biological Tests <87> Biological Reactivity Test, In Vitro—Elution Test Withdrawn and replaced with newer version. 2-159 2-186 USP 34-NF29:2011 Biological Tests <88> Biological Reactivity Tests, In Vivo, Procedure Preparation of Sample Withdrawn and replaced with newer version. 2-160 2-187 USP 34-NF29:2011 Biological Tests <88> Biological Reactivity Test, In Vitro, Classification of Plastics—Intracutaneous Test Withdrawn and replaced with newer version. 2-161 2-188 USP 34-NF29:2011 Biological Tests <88> Biological Reactivity Tests, In Vivo Classification of Plastics—Systemic Injection Test Withdrawn and replaced with newer version. 2-165 ANSI/AAMI/ISO 10993-14:2001 (Reapproved 2006) Biological evaluation of medical devices—Part 14: Identification and quantification of degradation products from ceramics Reaffirmation. 2-166 2-180 ANSI/AAMI/ISO 10993-16:2010 Biological evaluation of medical devices—Part 16: Toxicokinetic study design for degradation products and leachables Withdrawn and replaced with newer version. C. Cardiovascular 3-52 ANSI/AAMI EC12:2000/(R)2010 Disposable ECG electrodes Reaffirmation. 3-61 3-95 IEC 60601-2-27 Edition 3.0 2011-03 Medical electrical equipment—Part 2-27: Particular requirements for the basic safety and essential performance of electrocardiographic monitoring equipment Newer version with transition period. D. Dental/ENT 4-76 ISO 7785-2 Second edition 1995-08-01 Dental handpieces—Part 2: Straight and geared angle handpieces Contact person. 4-83 ISO 11498 First edition 1997-02-15 Dental handpieces—Dental low-voltage electrical motors Contact person. 4-84 ISO 13294 First edition 1997-05-01 Dental handpieces—Dental air-motors Contact person. 4-90 ANSI S3.39 Reaffirmed by ANSI May 18, 2007 Specifications for Instruments to Measure Aural Acoustic Impedance and Admittance (Aural Acoustic Immittance) Contact person. 4-119 ANSI/ADA Specification No. 82-1998 (R2009) Reversible/Irreversible Hydrocolloid Impression Material Systems Reaffirmation. 4-121 ISO 7494-2 First edition 2003-03-01 Dentistry—Dental units—Part 2: Water and air supply Contact person. 4-123 ANSI/ASA S3.6-2004 Specification for Audiometers Contact person. 4-126 ISO 10477 Second edition 2004-10-01 Dentistry—Polymer-based crown and bridge materials Contact person. 4-134 ISO 7494-1 First edition 2004-08-15 Dentistry—Dental units—Part 1: General requirements and test methods Contact person. 4-136 ASTM Designation: F2504-05 Standard Practice for Describing System Output of Implantable Middle Ear Hearing Devices Contact person. 4-150 ANSI/ADA Specification No. 19-2003 Dental Elastometric Impression Material:2003 Contact person. 4-154 ISO 4823 Third edition 2000-12-15 Dentistry—Elastometric impression materials Contact person. 4-155 ISO 4823:2000 Technical Corrigendum 1 Published 2004-07-15 Dentistry—Elastomeric impression materials Contact person. 4-156 ISO 4823 Third edition 2000-12-15 Amendment 1 2007-07-01 Dentistry—Elastometric impression materials Contact person. 4-160 ANSI S3.1-1999 (Reaffirmed by ANSI October 28, 2008) American National Standard Maximum Permissible Ambient Noise Levels for Audiometric Test Rooms Contact person. 4-162 ANSI S3.4-2007 American National Standard Procedure for the Computation of Loudness of Steady Sounds Contact person. 4-163 ANSI S3.5-1997 (R1986) Reaffirmed by ANSI May 18, 2007 American National Standard Methods for Calculation of the Speech Intelligibility Index Contact person. 4-164 ANSI S3.7-1995 (Reaffirmed by ANSI October 28, 2008) American National Standard Method for Coupler Calibration of Earphones Contact person. 4-165 ANSI S3.13-1987 Reaffirmed by ANSI June 1, 2007 American National Standard Mechanical Coupler for Measurement of Bone Vibrators Contact person. 4-170 ANSI S3.36-1985 Reaffirmed by ANSI on 4/27/2006 American National Standard Specification for a Manikin for Simulated in-situ Airborne Acoustic Measurements Contact person. 4-171 ANSI S3.37-1987 (Reaffirmed by ANSI May 18, 2007) American National Standard Preferred Earhook Nozzle Thread for Postauricular Hearing Aids Contact person. 4-172 ANSI S3.42-1992 Reaffirmed by ANSI May 18, 2007 American National Standard Testing Hearing Aids with a Broad-Band Noise Signal Contact person. 4-173 ANSI S3.44-1996 Reaffirmed by ANSI on 27 April 2006 American National Standard Determination of Occupational Noise Exposure and Estimation of Noise-Induced Hearing Impairment Contact person. 4-175 ANSI S3.46-1997 American National Standard Methods of Measurement of Real-Ear Performance Characteristics of Hearing Aids Contact person. 4-177 ANSI S12.65-2006 (Reaffirmed by ANSI March 30, 2011) American National Standard For Rating Noise with Respect to Speech Interference Reaffirmation. 4-179 ISO 7405 Second edition 2008-12-15 Dentistry—Evaluation of biocompatibility of medical devices used in dentistry Contact person. 4-180 ISO 9168 Third edition 2009-07-15 Dentistry—Hose connectors for air driven dental handpieces Contact person. 4-183 ANSI S3.2-2009 American National Standard Method for Measuring the Intelligibility of Speech over Communication Systems Contact person. 4-184 ANSI/ASA S3.25-2009 American National Standard For an Occluded Ear Simulator Contact person. 4-185 ANSI/ASA S3.45-2009 American National Standard Procedures for Testing Basic Vestibular Function Contact person. 4-186 ANSI/ASA S12.2-2008 American National Standard Criteria for Evaluating Room Noise Contact person. 4-190 ANSI/ASA S3.35-2010 American National Standard Method of Measurement of Performance Characteristics of Hearing Aids Under Simulated Real-Ear Working Conditions Contact person. 4-192 ANSI/ADA Specification No. 58-2010 Root Canal Files Type H (Hedstrom): 2007 Contact person. E. General 5-29 AAMI/ANSI HE74-2001 (R 2009) Human factors design process for medical devices Withdrawn, see 5-67. 5-39 IEC 60812 Second edition 2006-01 Analysis techniques for system reliability—Procedure for failure mode and effects analysis (FMEA) Contact person. 5-40 ISO 14971 Second edition 2007-03-01 Medical devices—Application of risk management to medical devices Contact person. 5-42 ASTM D903-98 (Reapproved 2010) Standard Test Methods for Peel or Stripping Strength of Adhesive Bonds Reaffirmation. 5-58 IEC 60601-1-11 Edition 1.0:2010 Medical electrical equipment—Part 1-11: General requirements for basic safety and essential performance—Collateral Standard: Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment Extent of recognition and relevant guidance. F. General Hospital/General Plastic Surgery 6-117 ASTM F2172-02(2011) Standard Specification for Blood/Intravenous Fluid/Irrigation Fluid Warmers Reaffirmation and Contact person. 6-161 ISO 10555-1 First edition 1995-06-15 Sterile, Single-use intravascular catheters—Part 1: General requirements Title and Contact person. 6-164 ISO 10555-5 First edition 1996-06-15 Sterile, single-use intravascular catheters—Part 5: Over-needle peripheral catheters Title and Contact person. 6-164 6-266 ISO 10555-5 First edition 1996-06-15 AMENDMENT 1 1999-01-15 Corrected and reprinted 1999-07-15 Sterile, single-use intravascular catheters—Part 5: Over-needle peripheral catheters See 6-164. 6-164 6-267 ISO 10555-5:1996 TECHNICAL CORRIGENDUM 1 Published 2002-06-15 Sterile, single-use intravascular catheters—Part 5: Over-needle peripheral catheters TECHNICAL CORRIGENDUM See 6-164. 6-176 ASTM D7103-06 1 Standard Guide for Assessment of Medical Gloves Editorial change. 6-177 ASTM E1112-00 (Reapproved 2011) Standard Specification for Electronic Thermometer for Intermittent Determination of Patient Temperature Reaffirmation. 6-198 6-254 ASTM F2100-11, Standard Specification for Performance of Materials Used in Medical Face Masks Withdrawn and replaced with newer version. 6-203 ASTM D6499-07, Standard Test Method for The Immunological Measurement of Antigenic Protein in Natural Rubber and its Products Extent of recognition. 6-219 6-255 USP 34-NF 29<11>:2011 Sodium Chloride Irrigation Withdrawn and replaced with newer version. 6-226 6-256 USP 34-NF 29<11>:2011 Sodium Chloride Injection Withdrawn and replaced with newer version. 6-246 6-257 USP 34-NF 29 2011 Nonabsorbable Surgical Suture Withdrawn and replaced with newer version. 6-248 6-258 USP 34-NF 29 2011 <881> Tensile Strength Withdrawn and replaced with newer version. 6-249 6-259 USP 34-NF 29 2011 <861> Sutures Diameter Withdrawn and replaced with newer version. 6-250 6-260 USP 34-NF 29 2011 <871> Sutures—Needle Withdrawn and replaced with newer version. 6-251 6-261 USP 34-NF 29 <11>:2011 Sterile Water for Irrigation Withdrawn and replaced with newer version. 6-252 6-262 USP 34-NF 29 <11>:2011 Heparin Lock Flush Solution Withdrawn and replaced with newer version. G. In Vitro Diagnostics 7-102 7-221 CLSI H01-A6 Tubes and Additives for Venous and Capillary Blood Specimen Collection; Approved Standard—Sixth Edition Withdrawn and replaced with newer version. 7-112 CLSI H49-A Point-of-Care Monitoring of Anticoagulation Therapy; Approved Guideline Withdrawn duplicate, see 7-162. 7-126 7-222 CLSI M24-A2 Susceptibility Testing of Mycobacteria, Nocardiae, and Other Aerobic Actinomycetes; Approved Standards—Second Edition Withdrawn and replaced with newer version Contact person. 7-128 CLSI EP14-A2 Evaluation of Matrix Effects; Approved Guideline—Second Edition Withdrawn duplicate, see 7-143. 7-130 CLSI H20-A2 Reference Leukocyte (WBC) Differential Count (Proportional) and Evaluation of Instrumental Methods; Approved Standard—Second Edition Withdrawn duplicate, see 7-165. 7-134 CLSI GP20-A2 Fine Needle Aspiration Biopsy (FNAB) Techniques; Approved Guideline—Second Edition Withdrawn duplicate, see 7-166. 7-140 7-223 GP22-A3—Quality Management System: Continual Improvement; Approved Guideline—Third Edition Withdrawn and replaced with newer version. 7-143 CLSI EP14-A2 Evaluation of Matrix Effects; Approved Guideline—Second Edition Contact person, Type of standard, Processes impacted. 7-147 CLSI M22-A3 Quality Control for Commercially Prepared Microbiological Culture Media; Approved Standard—Third Edition Withdrawn duplicate, see 7-178. 7-150 CLSI H43-A2 Clinical Flow Cytometric Analysis of Neoplastic Hematolymphoid Cells; Approved Guideline—Second Edition Title, Contact person. 7-162 CLSI H49-A Point-of-Care Monitoring of Anticoagulation Therapy; Approved Guideline Contact person, Devices affected, Processes affected, Type of standard, CFR citation and product codes. 7-165 CLSI H20-A2 Reference Leukocyte (WBC) Differential Count (Proportional) and Evaluation of Instrumental Methods; Approved Standard—Second Edition Contact person, Devices affected, Processes affected, Type of standard, CFR citation and product codes. 7-166 CLSI GP20-A2 Fine Needle Aspiration Biopsy (FNAB) Techniques; Approved Guideline—Second Edition Devices affected, Process affected, CFR citation and product codes. 7-169 CLSI M27-A3 Reference Method for Broth Dilution Antifungal Susceptibility Testing of Yeasts; Approved Standard—Third Edition Withdrawn duplicate, see 7-204. 7-172 CLSI C28-A3 Defining, Establishing, and Verifying Reference Intervals in the Clinical Laboratory; Approved Guideline—Third Edition Withdrawn duplicate, see 7-224. 7-202 7-224 CLSI C28-A3c Defining, Establishing, and Verifying Reference Intervals in the Clinical Laboratory; Approved Guideline—Third Edition Withdrawn and replaced with newer version. 7-178 CLSI M22-A3 Quality Control for Commercially Prepared Microbiological Culture Media; Approved Standard—Third Edition Extent of recognition, CFR citation and product codes. 7-204 CLSI M27-A3 Reference Method for Broth Dilution Antifungal Susceptibility Testing of Yeasts; Approved Standard—Third Edition Contact person. 7-206 CLSI I/LA 20-A2 Analytical Performance Characteristics and Clinical Utility of Immunological Assays for Human Immunoglobulin E (IgE) Antibodies and Defined Allergen Specificities; Approved Guideline—Second Edition Title, Contact person. H. Materials 11-219 8-203 ASTM F2026-08 Standard Specification for Polyetheretherketone (PEEK) Polymers for Surgical Implant Applications Transferred. 8-101 8-204 ASTM F2118-10 Standard Test Method for Constant Amplitude of Force Controlled Fatigue Testing of Acrylic Bone Cement Materials Withdrawn and replaced with newer version. 8-105 8-205 ASTM F1635-11 Standard Test Method for in vitro Degradation Testing of Hydrolytically Degradable Polymer Resins and Fabricated Forms for Surgical Implants Withdrawn and replaced with newer version. 8-114 ASTM F2255-05 (Reapproved 2010) Standard Test Method for Strength Properties of Tissue Adhesives in Lap-Shear by Tension Loading Reaffirmation. 8-115 ASTM F2256-05 (Reapproved 2010) Standard Test Method for Strength Properties of Tissue Adhesives in T-Peel by Tension Loading Reaffirmation. 8-116 ASTM F2258-05 (Reapproved 2010) Standard Test Method for Strength Properties of Tissue Adhesives in Tension Reaffirmation. 8-119 8-206 ASTM F688-10 Standard Specification for Wrought Cobalt-35 Nickel-20 Chromium-10 Molybdenum Alloy Plate, Sheet, and Foil for Surgical Implants (UNS R30035) Withdrawn and replaced with newer version. 8-121 ASTM F2005-05 (Reapproved 2010) Standard Terminology for Nickel-Titanium Shape Memory Alloys Reaffirmation. 8-125 ASTM F2004-05 (Reapproved 2010) Standard Test Method for Transformation Temperature of Nickel-Titanium Alloys by Thermal Analysis Reaffirmation. 8-126 ASTM F561-05a (Reapproved 2010) Standard Practice for Retrieval and Analysis of Medical Devices, and Associated Tissues and Fluids Reaffirmation. 8-132 ASTM F1088-04a (Reapproved 2010) Standard Specification for Beta-Tricalcium Phosphate for Surgical Implantation Reaffirmation and contact person. 8-135 ASTM F2392-04 (Reapproved 2010) Standard Test Method for Burst Strength of Surgical Sealants Reaffirmation. 8-136 ASTM F2458-05 (Reapproved 2010) Standard Test Method for Wound Closure Strength of Tissue Adhesives and Sealants Reaffirmation. 8-172 8-207 ASTM F1926/F1926M-10 Standard Test Method for Evaluation of the Environmental Stability of Calcium Phosphate Granules, Fabricated Forms, and Coatings Withdrawn and replaced with newer version. 8-178 8-208 ASTM F648-10a Standard Specification for Ultra-High-Molecular-Weight Polyethylene Powder and Fabricated Form for Surgical Implants Withdrawn and replaced with newer version. 8-181 8-209 ASTM F899-11 Standard Specification for Wrought Stainless Steels for Surgical Instruments Withdrawn and replaced with newer version. 8-191 8-210 ASTM F2182-11 Standard Test Method for Measurement of Radio Frequency Induced Heating On or Near Passive Implants During Magnetic Resonance Imaging Withdrawn and replaced with newer version. 8-195 ASTM F2024-10, Standard Practice for X-Ray Diffraction Determination of Phase Content of Plasma-Sprayed Hydroxyapatite Coatings Extent of Recognition, devices affected, CFR citations and associated procodes and contact person. I. Neurology 17-1 ANSI/AAMI NS28:1988/(R) 2010 Intracranial pressure monitoring devices Reaffirmation. 17-3 ISO 7197:2006 Third edition 2006-06-01 Neurosurgical implants—Sterile, single-use hydrocephalus shunts and components Contact person. 17-4 ASTM F 647-94 (Reapproved 2006) Standard Practice for Evaluating and Specifying Implantable Shunt Assemblies for Neurosurgical Application Contact person. 17-7 ISO 7197:2006 Technical Corrigendum 1 Published:2007-07-01 Neurological implants—Sterile, single-use hydrocephalus shunts and components Contact person. J. OB-GYN/Gastroenterology 9-21 ISO 8600-4 First edition 1997-07-01 Optics and optical instruments—Medical endoscopes and certain accessories—Part 4: Determination of maximum width of insertion portion Contact person. 9-37 ISO 8600-1 Second edition 2005-05-01 Optics and photonics—Medical endoscopes and endotherapy devices—Part 1: General requirements Contact person. 9-38 ISO 8600-3 First edition 1997-07-01 AMENDMENT 1 2003-12-01 Optics and optical instruments—Medical endoscopes and endoscopic accessories Part 3: Determination of field of view and direction of view of endoscopes with optics Contact person. 9-39 ISO 8600-5 First edition 2005-03-15 Optics and photonics—Medical endoscopes and endotherapy devices—Part 5: Determination of optical resolution of rigid endoscopes with optics Contact person. 9-40 ISO 8600-6 First edition 2005-03-15 Optics and photonics—Medical endoscopes and endotherapy devices—Part 6: Vocabulary Contact person. 9-44 ASTM Designation: F 623-99 (Reapproved 2006) Standard Performance Specification for Foley Catheter Contact person. 9-49 AAMI/ANSI RD61:2006, Concentrates for hemodialysis Withdrawn, see 9-73. 9-50 ANSI/AAMI RD52:2004/(R)2010 Dialysate for Hemodialysis Withdrawn, see 9-70 and 9-71. 9-53 ASTM F 1992-99 (Reapproved 2007) Standard Practice for Reprocessing of Reusable, Heat-Stable Endoscopic Accessory Instruments (EAI) Used with Flexible Endoscopes Contact person. 9-55 AAMI/ANSI RD62:2006 and ANSI/AAMI RD62:2006/A1:2009, Water treatment equipment for hemodialysis applications Withdrawn, see 9-69. 9-61 IEC 60601-2-18 Edition 3.0 2009-08 Medical electrical equipment—Part 2-18: Particular requirements for the basic safety and essential performance of endoscopic equipment Contact person. 9-59 AAMI/ANSI RD5:2003/(R)2008, Hemodialysis Withdrawn, see 9-72. K. Ophthalmic 10-15 ISO 9394 Second edition 1998-08-15 Ophthalmic optics—Contact lenses and contact lens care products—Determination of biocompatibility by ocular study using rabbit eyes Contact person. 10-24 10-67 ISO 11986 Second edition 2010-11-01 Ophthalmic optics—Contact lenses and contact lens care products—Determination of preservative uptake and release Withdrawn and replaced with newer version. 10-26 10-68 ISO 13212 Second edition 2011-05-15 Ophthalmic optics—Contact lens care products—Guidelines for determination of shelf-life Withdrawn and replaced with newer version. 10-28 ISO 14729 First edition 2001-04-15 Ophthalmic optics—Contact lens care products—Microbiological requirements and test methods for products and regimens for hygienic management of contact lenses Contact person. 10-29 ISO 14730 First edition 2000-09-15 Ophthalmic optics—Contact lens care products—Antimicrobial preservative efficacy testing and guidance on determining discard date Contact person. 10-33 10-69 ANSI Z80.18-2010 for Ophthalmics—Contact Lens Care Products—Vocabulary, Performance Specifications, and Test Methodology Withdrawn and replaced with newer version. 10-38 10-70 ISO 10943 Third edition 2011-08-15 Ophthalmic instruments—Indirect ophthalmoscopes Withdrawn and replaced with newer version. 10-59 ISO 11980 Second edition 2009-10-15 Ophthalmic optics—Contact lenses and contact lens care products—Guidance for clinical investigations Contact person. L. Orthopedic 11-167 11-226 ASTM F1089-10 Standard Test Method for Corrosion of Surgical Instruments Withdrawn and replaced with newer version. 11-180 11-227 ASTM F366-10 Standard Specification for Fixation Pins and Wires Withdrawn and replaced with newer version; change contact. 11-196 ASTM F1672-95 (Reapproved 2011) Standard Specification for Resurfacing Patellar Prosthesis Reaffirmation. 11-201 11-228 ASTM F564-10 Standard Specification and Test Methods for Metallic Bone Staples Withdrawn and replaced with newer version. 11-217 11-229 ASTM F2083-10 Standard Specification for Total Knee Prosthesis Withdrawn and replaced with newer version. 11-221 11-230 ASTM F1717-10 Standard Test Methods for Spinal Implant Constructs in a Vertebrectomy Model Withdrawn and replaced with newer version. 11-155 11-231 ISO 7207-2 Second edition 2011-07-01 Implants for surgery—Components for partial and total knee joint prostheses—Part 2: Articulating surfaces made of metal, ceramic and plastics materials Withdrawn and replaced with newer version. 11-219 8-203 ASTM F2026-10 Standard Specification for Polyetheretherketone (PEEK) Polymers for Surgical Implant Applications Transferred and replaced with a newer version. M. Radiology 12-52 UL 544 (1998), Standard for Medical and Dental Equipment—Ed. 4.0 Withdrawn, see 5-4 and 5-52. 12-62 UL 187 (1998), Standard for X-ray Equipment—Ed. 7.0 Withdrawn, see 5-4 and 5-52. 12-100 NEMA UD 3-2004 (R2009), Standard for Real Time Display of Thermal and Mechanical Acoustic Output Indices on Diagnostic Ultrasound Equipment, Revision 2 Reaffirmation. 12-105 NEMA UD 2-2004 (R2009), Acoustic Output Measurement Standard for Diagnostic Ultrasound Equipment, Revision 3 Reaffirmation. 12-106 ISO 17526 First edition 2003-06-15, Optics and optical instruments—Lasers and laser-related equipment—Lifetime of lasers Contact person. 12-108 12-246 ISO 21254-2 First edition 2011-07-15 Lasers and laser-related equipment—Test methods for laser-induced damage threshold—Part 2: Threshold determination Withdrawn and replaced with newer version. 12-109 12-245 ISO 21254-1 First edition 2011-07-15 Lasers and laser-related equipment—Test methods for laser-induced damage threshold—Part 1: Definitions and general principles Withdrawn and replaced with newer version. 12-110 ISO 11551 Second edition 2003-12-01, Optics and optical instruments—Lasers and laser-related equipment—Test method for absorptance of optical laser components Contact person. 12-113 ISO 12005 Second edition 2003-04-01, Lasers and laser-related equipment—Test methods for laser beam parameters—Polarization Contact person. 12-115 ISO 13695 First edition 2004-06-01, Optics and photonics—Lasers and laser-related equipment—Test methods for the spectral characteristics of lasers Contact person. 12-117 ISO 15367-1 First edition 2003-09-15, Lasers and laser-related equipment—Test methods for determination of the shape of a laser beam wavefront—Part 1: Terminology and fundamental aspects Contact person. 12-134 ISO 11146-1 First edition 2005-01-15, Lasers and laser-related equipment—Test methods for laser beam widths, divergence angles and beam propagation ratios—Part 1: Stigmatic and simple astigmatic beams Contact person. 12-140 AIUM RTD2-2004, Standard for Real-Time Display of Thermal and Mechanical Acoustic Output Indices on Diagnostic Ultrasound Equipment Revision 2 Title. 12-142 ISO 11146-2 First edition 2005-02-15, Lasers and laser-related equipment—Test methods for laser beam widths, divergence angles and beam propagation ratios—Part 2: General astigmatic beams Contact person. 12-143 ISO 15367-2 First edition 2005-03-15, Lasers and laser-related equipment—Test methods for determination of the shape of a laser beam wavefront—Part 2: Shack-Hartman sensors Contact person. 12-144 12-247 ISO 11990-1 First edition 2011-08-01 Lasers and laser-related equipment—Determination of laser resistance of tracheal tubes—Part 1: Tracheal tube shaft Withdrawn and replaced with newer version. 12-154 12-248 ISO 21254-3 First edition 2011-07-15 Lasers and laser-related equipment—Test methods for laser-induced damage threshold—Part 3: Assurance of laser power (energy) handling capabilities Withdrawn and replaced with newer version. 12-155 ISO 11554 Third edition 2006-05-01, Optics and photonics—Lasers and laser-related equipment—Test methods for laser beam power, energy and temporal characteristics Contact person. 12-156 ISO 11670:2003 Technical Corrigendum 1 Published 2004-05-15, Lasers and laser-related equipment—Test methods for laser beam parameters—Beam positional stability Contact person. 12-157 ISO 13694:2000 Technical Corrigendum 1 Published 2005-11-01, Optics and optical instruments—Lasers and laser-related equipment—Test methods for laser beam power (energy) density distribution Contact person. 12-174 ISO 13697 First edition 2006-05-15, Optics and photonics—Lasers and laser-related equipment—Test methods for specular reflectance and regular transmittance of optical laser components Contact person. 12-175 ISO 24013 First edition 2006-11-15, Optics and photonics—Lasers and laser-related equipment—Measurement of phase retardation of optical components for polarized laser radiation Contact person. 12-177 12-249 ANSI/UL 122-2007 Standard for Photographic Equipment—Ed. 5.0 Withdrawn and replaced with newer version. 12-125 12-231 NEMA MS 5-2010, Determination of Slice Thickness in Diagnostic Magnetic Resonance Imaging Withdrawn and replaced with newer version. 12-151 12-232 NEMA MS 4-2010, Acoustic Noise Measurement Procedure for Diagnosing Magnetic Resonance Imaging Devices Withdrawn and replaced with newer version. 12-160 12-234 NEMA MS 12-2010, Quantification and Mapping of Geometric Distortion for Special Applications Withdrawn and replaced with newer version. 12-162 12-235 IEC 60731 Edition 3.0 2011-02, Amendment 1, Medical electrical equipment—Dosimeters with ionization chambers as used in radiotherapy Withdrawn and replaced with newer version. 12-178 12-236 IEC 60601-2-45 Edition 3.0 2011-02, Medical electrical equipment—Part 2-45: Particular requirements for the basic safety and essential performance of mammographic X-ray equipment and mammographic stereotactic devices Newer version with transition period. 12-191 12-237 IEC 62359 Edition 2.0 2010-10, Ultrasonics—Field characterization—Test methods for the determination of thermal and mechanical indices related to medical diagnostic ultrasonic fields Withdrawn and replaced with newer version. 12-218 12-238 NEMA PS 3.1-3.20 (2011), Digital Imaging and Communications in Medicine (DICOM) Set Withdrawn and replaced with newer version. N. Software/Informatics 13-11 13-30 CLSI AUTO3-A2 Laboratory Automation: Communications with Automated Clinical Laboratory Systems, Instruments, Devices, and Information Systems; Approved Standard, Second Edition 2009 Withdrawn and replaced with newer version. O. Sterility 14-135 AAMI/ANSI ST63:2002, Sterilization of health care products—Requirements for the development, validation and routine control of an industrial sterilization process for medical devices—Dry heat Withdrawn, see 14-339. 14-169 ASTM F2391-05 (Reapproved 2011) Standard Test Method for Measuring Package and Seal Integrity Using Helium as the Tracer Gas Reaffirmation. 14-170 14-313 ASTM F2475-11 Standard Guide for Biocompatibility Evaluation of Medical Device Packaging Materials Withdrawn and replaced with newer version. 14-181 ANSI/AAMI ST58:2005/(R)2010 Chemical sterilization and high-level disinfection in health care facilities Reaffirmation and contact person. 14-193 ANSI/AAMI/ISO 11607-1:2006/(R)2010 Packaging for terminally sterilized medical devices—Part 1: Requirements for materials, sterile barrier systems, and packaging systems Reaffirmation. 14-194 ANSI/AAMI/ISO 11607-2:2006/(R)2010 Packaging for terminally sterilized medical devices—Part 2: Validation requirements for forming, sealing, and assembly processes Reaffirmation. 14-195 ANSI/AAMI/ISO 11140-1:2005(R)2010 Sterilization of health care products—Chemical indicators—Part 1: General requirements Reaffirmation, extent of recognition, and type of standard. 14-201 ANSI/AAMI ST77:2006/(R)2010 Containment devices for reusable medical device sterilization Reaffirmation and contact person. 14-214 AOAC 6.2.04:2009 Official Method 955.15, Testing Disinfectants Against Staphylococcus aureus, Use—Dilution Method Reaffirmation. 14-216 AOAC 6.2.06:2009 Official Method 964.02, Testing Disinfectants Against Pseudomonas aeruginosa, Use—Dilution Method Reaffirmation. 14-219 AOAC 6.3.06:2008 Official Method 965.12, Tuberculocidal Activity of Disinfectants Reaffirmation. 14-222 ANSI/AAMI/ISO 18472:2006/(R)2010 Sterilization of health care products—Biological and chemical indicators—Test equipment Reaffirmation, and contact person. 14-225 ANSI/AAMI/ISO 11137-2:2006 Sterilization of health care products—Radiation—Part 2: Establishing the sterilization dose Extent of recognition and relevant guidance. 14-227 ANSI/AAMI/ISO 11737-1:2006 Sterilization of health care products—Microbiological methods—Part 1: Determination of the population of microorganisms on product Extent of recognition and title. 14-228 ANSI/AAMI/ISO 11135-1:2007 Sterilization of health care products—Ethylene oxide—Part 1: Requirements for development, validation, and routine control of a sterilization process for medical devices Extent of recognition. 14-238 ANSI/AAMI/ISO 11140-5:2007, Sterilization of health care products—Chemical indicators—Part 5: Class 2 indicators for Bowie and Dick-type air removal tests Relevant guidance. 14-261 ANSI/AAMI/ISO 17665-1:2006 Sterilization of health care products—Moist heat—Part 1: Requirements for the development, validation, and routine control of a sterilization process for medical devices Extent of recognition, relevant guidance and contact person. 14-274 ANSI/AAMI/ISO 15882:2008 Sterilization of health care products—Chemical indicators—Guidance for selection, use, and interpretation of results Extent of recognition. 14-276 14-314 ANSI/AAMI ST67:2011 Sterilization of health care products—Requirements and guidance for selecting a sterility assurance level (SAL) for products labeled “sterile” Withdrawn and replaced with newer version. 14-285 ANSI/AAMI/ISO 14161:2009 Sterilization of health care products—Biological indicators—Guidance for the selection, use and interpretation of results Title, contact person. 14-287 ANSI/AAMI/ISO 11737-2:2009 Sterilization of medical devices—Microbiological methods—Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process Extent of recognition and title. 14-291 ANSI/AAMI/ISO 14937:2009 Sterilization of health care products—General requirements for characterization of a sterilizing agent and the development, validation, and routine control of a sterilization process for medical devices Extent of recognition. 14-295 ANSI/AAMI ST81:2004/(R)2010, Sterilization of medical devices—Information to be provided by the manufacturer for the processing of resterilizable medical devices Relevant guidance and contact person. 14-296 ANSI/AAMI/ISO 11138-1:2006/(R)2010 Sterilization of health care products—Biological indicators—Part 1: General requirements Extent of recognition, contact person and relevant guidance. 14-297 ANSI/AAMI/ISO 11137-1:2006/(R)2010 Sterilization of health care products—Radiation—Part 1: Requirements for development, validation, and routine control of a sterilization process for medical devices Extent of recognition, and relevant guidance. 14-298 ANSI/AAMI/ISO 11137-3:2006/(R)2010 Sterilization of health care products—Radiation—Part 3: Guidance on dosimetric aspects Extent of recognition and relevant guidance. 14-301 14-315 USP 34:2011 <61> Microbiological Examination of Nonsterile Products: Microbial Enumeration Tests Withdrawn and replaced with newer version. 14-302 14-316 USP 34:2011 <71> Sterility Tests Withdrawn and replaced with newer version. 14-303 14-317 USP 34:2011 <85> Bacterial Endotoxins Test Withdrawn and replaced with newer version. 14-304 14-318 USP 34:2011 <151> Pyrogen Test (USP Rabbit Test) Withdrawn and replaced with newer version. 14-305 14-319 USP 34:2011 <161> Transfusion and Infusion Assemblies and Similar Medical Devices Withdrawn and replaced with newer version. 14-306 14-320 USP 34:2011 Biological Indicator for Steam Sterilization—Self Contained Withdrawn and replaced with newer version. 14-307 14-321 USP 34:2011 Biological Indicator for Dry-Heat Sterilization, Paper Carrier Withdrawn and replaced with newer version. 14-308 14-322 USP 34:2011 Biological Indicator for Ethylene Oxide Sterilization, Paper Carrier Withdrawn and replaced with newer version. 14-309 14-323 USP 34:2011 Biological Indicator for Steam Sterilization, Paper Carrier Withdrawn and replaced with newer version. 14-310 14-324 USP 34:2011 <62> Microbiological Examination of Nonsterile Products: Tests for Specified Microorganisms Withdrawn and replaced with newer version. P. Tissue Engineering 15-7 15-27 ASTM F2315-11 Standard Guide for Immobilization or Encapsulation of Living Cells or Tissue in Alginate Gels Withdrawn and replaced with newer version. 15-8 ASTM F2064-00 (Reapproved 2006) 1 Standard Guide for Characterization and Testing of Alginates as Starting Materials Intended for Use in Biomedical and Tissue-Engineered Medical Products Application Editorial change. 15-10 ASTM F2451-05 (Reapproved 2010) Standard Guide for in vivo Assessment of Implantable Devices Intended to Repair or Regenerate Articular Cartilage Reaffirmation. 15-12 15-28 ASTM F2103-11 Standard Guide for Characterization and Testing of Chitosan Salts as Starting Materials Intended for Use in Biomedical and Tissue-Engineered Medical Product Applications Withdrawn and replaced with newer version. 15-15 15-29 ASTM F2259-10 Standard Test Method for Determining the Chemical Composition and Sequence in Alginate by Proton Nuclear Magnetic Resonance (1H NMR) Spectroscopy Withdrawn and replaced with newer version. 15-18 15-30 ASTM F2212-11 Standard Guide for Characterization of Type I Collagen as Starting Material for Surgical Implants and Substrates for Tissue Engineered Medical Products (TEMPs) Withdrawn and replaced with newer version. 15-25 15-31 ASTM F2312-11 Standard Terminology Relating to Tissue Engineered Medical Products Withdrawn and replaced with newer version. 1 All standard titles in this table conform to the style requirements of the respective organizations. In table 3 of this document, FDA provides the listing of new entries and consensus standards added as modifications to the list of recognized standards under Recognition List Number: 028. Table 3—New Entries to the List of Recognized Standards Recognition No. Title of standard 1 Reference Number and date A. Biocompatibility 2-173 Biological evaluation of medical devices—Part 10: Tests for irritation and skin sensitization ANSI/AAMI/ISO 10993-10:2010. 2-175 Biological evaluation of medical devices Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity ISO 10993-3 Second edition 2003-10-15. 2-176 Biological evaluation of medical devices Part 11: Tests for systemic toxicity ISO 10993-11 Second edition 2006-08-15. 2-177 Biological evaluation of medical devices—Part 6: Tests for local effects after implantation ISO 10993-6 Second edition 2007-04-15. 2-178 Biological evaluation of medical devices—Part 12: Sample preparation and reference materials ISO 10993-12 Third edition 2007-11-15 Corrected version 2008-02-15. 2-179 Biological evaluation of medical devices—Part 1: Evaluation and testing within a risk management process ISO 10993-1 Fourth edition 2009-10-15. 2-181 Clinical investigation of medical devices for human subjects—Good clinical practice ANSI/AAMI/ISO 14155:2011. 2-182 Clinical investigation of medical devices for human subjects—Good clinical practice ISO 14155 Second edition 2011-02-01. 2-183 Clinical investigation of medical devices for human subjects—Good clinical practice TECHNICAL CORRIGENDUM 1 ISO 14155: 2011 Technical Corrigendum 1 Published 2011-07-15. B. Cardiovascular 3-96 Non-invasive sphygmomanometers—Part 1: Requirements and test methods for non-automated measurement type ISO 81060-1 First edition 2007-12-01. 3-97 Non-invasive sphygmomanometers—Part 2: Clinical validation of automated measurement type ISO 81060-2 First edition 2009-05-01. 3-98 Non-invasive sphygmomanometers—Part 2: Clinical validation of automated measurement type TECHNICAL CORRIGENDUM 1 ISO 81060-2:2009 TECHNICAL CORRIGENDUM 1 Published 2011-02-15. 3-99 Evaluation of particulates associated with vascular medical devices AAMI TIR42:2010. 3-100 Medical electrical equipment—Part 2-27: Particular requirements for the basic safety and essential performance of electrocardiographic monitoring equipment ANSI/AAMI/IEC 60601-2-27:2011. C. General 5-68 Medical devices—Symbols to be used with medical device labels, labelling, and information to be supplied—Part 2: Symbol development, selection and validation ANSI/AAMI/ISO 15223-2:2010. 5-69 Medical electrical equipment—Part 1-11: General requirements for basic safety and essential performance—Collateral Standard: Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment Corrigendum 1 IEC 60601-1-11 (First edition—2010) April 2011. 5-70 Medical devices—Application of risk management to medical devices ANSI/AAMI/ISO 14971:2007/(R)2010. D. General Hospital/General Plastic Surgery 6-263 Absorbable Surgical Suture USP 34-NF 28 2011. 6-264 Sterile, single-use intravascular catheters—Part 1: General requirements ISO 10555-1 First edition 1995-06-15 Amendment 1 1999-07-15. 6-265 Sterile, single-use intravascular catheters—Part 1: General requirements ISO 10555-1 First edition 1995-06-15 AMENDMENT 2 2004-05-15. 6-268 Standard Terminology Relating to Hemostatic Forceps ASTM F921—10 (Reapproved 2011). 6-269 Standard Terminology for Surgical Scissors—Inserted and Non-Inserted Blades ASTM F1078—10 (Reapproved 2011). 6-270 Standard Terminology for Surgical Suture Needles ASTM F1840-10 1 . 6-271 Standard Test Method for Bend Testing of Needles Used in Surgical Sutures ASTM F1874—98 (Reapproved 2011). 6-272 Standard Specification for Square Drive Interconnections on Surgical Instruments ASTM F2062—00 (Reapproved 2011). 6-273 Sharps injury protection—Requirements and test methods—Sharps protection features for single-use hypodermic needles, introducers for catheters and needles used for blood sampling ISO 23908 First edition 2011-06-11. E. In Vitro Diagnostics 7-225 Validation and Verification of Tubes for Venous and Capillary Blood Specimen Collection; Approved Guideline CLSI GP34-A. 7-226 Quality Management System: A Model for Laboratory Services; Approved Guideline—Fourth Edition CLSI GP26-A4. 7-227 Criteria for Laboratory Testing and Diagnosis of Human Immunodeficiency Virus Infection; Approved Guideline CLSI M53-A. F. Materials 8-211 Implants for surgery—Ultra-high-molecular-weight polyethylene—Part 1: Powder form ISO 5834-1 Third edition 2005-06-01. 8-212 Implants for surgery—Ultra-high-molecular-weight polyethylene—Part 1: Powder form TECHNICAL CORRIGENDUM 1 ISO 5834-1:2005 TECHNICAL CORRIGENDUM 1 Published 2007-05-01. 8-213 Implants for surgery—Ultra-high-molecular-weight polyethylene—Part 3: Accelerated ageing methods ISO 5834-3 First edition 2005-07-15. 8-214 Implants for surgery—Ultra-high molecular weight polyethylene—Part 4: Oxidation index measurement method ISO 5834-4 First edition 2005-05-01. 8-215 Implants for surgery—Ultra-high-molecular-weight polyethylene—Part 5: Morphology assessment method ISO 5834-5 First edition 2005-06-01. G. Neurology 17-9 Implants for surgery—Active implantable medical devices Part 3: Implantable neurostimulators ANSI/AAMI/ISO 14708-3:2008. H. OB-GYN/Gastroenterology 9-69 Water for hemodialysis and related therapies ANSI/AAMI/ISO 13959:2009. 9-70 Guidance for the preparation and quality management of fluids for hemodialysis and related therapies ANSI/AAMI/ISO 23500:2011. 9-71 Quality of dialysis fluid for hemodialysis and related therapies ANSI/AAMI/ISO 11663:2009. 9-72 Medical electrical equipment, Part 2-16: Particular requirements for basic safety and essential performance of hemodialysis, hemodiafiltration and hemofiltration equipment ANSI/AAMI/IEC 60601-2-16:2008. 9-73 Concentrates for haemodialysis and related therapies ANSI/AAMI/ISO 13958:2009. 9-74 Concentrates for haemodialysis and related therapies ISO 13958 Second edition 2009-4-15. I. Ophthalmic 10-71 Ophthalmic optics—Contact lens care products—Microbiological requirements and test methods for products and regimens for hygienic management of contact lenses ISO 14729 First edition 2001-04-15 AMENDMENT 1 2010-10-01. 10-72 Ophthalmic instruments—Fundamental requirements and test methods—Part 1: General requirements applicable to all ophthalmic instruments ISO 15004-1 First edition 200-606-01. J. Orthopedic 11-232 Implants for surgery—Components for partial and total knee joint prostheses—Part 1: Classification, definitions and designation of dimensions ISO 7207-1 Third edition 2007-02-01. 11-233 Standard Specifications and Test Methods for Metallic Angled Orthopedic Fracture Fixation Devices ASTM F384—06 (Reapproved 2011). 11-234 Standard Test Method for Wear Testing of Polymeric Materials Used in Total Joint Prostheses ASTM F732—00 (Reapproved 2011). K. Radiology 12-233 Lasers and laser-related equipment—Test methods for laser beam parameters—Beam positional stability ISO 11670 Second edition 2003-04-01. 12-239 SAFETY OF LASER PRODUCTS—Part 1: Equipment classification and requirements, INTERPRETATION SHEET 1 IEC 60825-1 (Second edition—2007) I-SH 01 December 2009. 12-240 SAFETY OF LASER PRODUCTS—Part 1: Equipment classification and requirements, INTERPRETATION SHEET 2 IEC 60825-1 (2007), second edition/I-SH 02 January 2011. 12-241 Medical electrical equipment—Safety of radiotherapy record and verify systems IEC 62274 First edition 2005-05. 12-242 Medical electrical equipment—Part 2-57: Particular requirements for the basic safety and essential performance of non-laser light source equipment intended for therapeutic, diagnostic, monitoring and cosmetic/aesthetic use IEC 60601-2-57 Edition 1.0 2011-01. 12-243 Optics and optical instruments—Lasers and laser-related equipment—Test methods for laser beam power [energy] density distribution ISO 13694, First edition 2000-04-01. 12-244 Ultrasonics—Field characterization—Test methods for the determination of thermal and mechanical indices related to medical diagnostic ultrasonic fields CORRIGENDUM 1 IEC 62359 (Second edition—2010). L. Sterility 14-325 Sterilization of health care products—Vocabulary ISO/TS 11139 Second edition 2006-01-15. 14-326 Sterilization of medical devices—Microbiological methods—Part 1: Determination of a population of microorganisms on products ISO 11737-1 Second edition 2006-04-01. 14-327 Sterilization of medical devices—Microbiological methods—Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process ISO 11737-2 Second edition 2009-11-15. 14-328 Sterilization of health care products—Radiation—Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices ISO 11137-1 First edition 2006-04-15. 14-329 Sterilization of health care products—Radiation—Part 2: Establishing the sterilization dose ISO 11137-2 First edition 2006-04-15. 14-330 Sterilization of health care products—Radiation—Part 3: Guidance on dosimetric aspects ISO 11137-3 First edition 2006-04-15. 14-331 Sterilization of health care products—Ethylene oxide—Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices ISO 11135-1 First edition 2007-05-01. 14-332 Sterilization of health care products—Chemical indicators—Part 5: Class 2 indicators for Bowie and Dick-type air removal tests ISO 11140-5 Second edition 2007-03-15. 14-333 Sterilization of health care products—Moist heat—Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices ISO 17665-1 First edition 2006-08-15. 14-334 Sterilization of health care products—Chemical indicators—Guidance for selection, use and interpretation of results ISO 15882 Second edition 2008-09-01. 14-335 Biological evaluation of medical devices—Part 7: Ethylene oxide sterilization residuals ISO 10993-7 Second edition 2008-10-15. 14-336 Sterilization of health care products—Biological indicators—Guidance for the selection, use and interpretation of results ISO 14161 Second edition 2009-09-15. 14-337 Sterilization of health care products—General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices ISO 14937 Second edition 2009-10-15. 14-338 Sterilization of health care products—Biological indicators—Part 1: General requirements ISO 11138-1 Second edition 2006-07-01. 14-339 Sterilization of health care products—Dry heat—Requirements for the development, validation and routine control of a sterilization process for medical devices ANSI/AAMI/ISO 20857:2010. 14-340 Sterilization of health care products—Dry heat—Requirements for the development, validation and routine control of a sterilization process for medical devices ISO 20857 First edition 2010-08-15. 14-341 Standard Guide for Absorbed-Dose Mapping in Radiation Processing Facilities ASTM E2303—11. 14-342 Standard Practice for Dosimetry in Radiation Processing ASTM E2628—09 1 . 14-343 Standard Guide for Performance Characterization of Dosimeters and Dosimetry Systems for Use in Radiation Processing ASTM E2701—09. 14-344 Standard Practice for Climatic Stressing of Packaging Systems for Single Parcel Delivery ASTM F2825—10 1 . 14-345 Standard guide for selection and calibration of dosimetry systems for radiation processing ISO/ASTM 51261 First edition 2002-03-15. 14-346 Standard Practice for Use of a Polymethylmethacrylate Dosimetry System ISO/ASTM 51276 Second edition 2002-12-15. 14-347 Standard Practice for Dosimetry in Gamma Irradiation Facilities for Radiation Processing ISO/ASTM 51702 Second edition 2004-08-15. 14-348 Aseptic processing of health care products—Part 2: Filtration ANSI/AAMI/ISO 13408-2:2003. 14-349 Aseptic processing of health care products—Part 3: Lyophilization ANSI/AAMI/ISO 13408-3:2006. 14-350 Aseptic processing of health care products—Part 4: Clean-in-place technologies ANSI/AAMI/ISO 13408-4:2005. 14-351 Aseptic processing of health care products—Part 5: Sterilization in place ANSI/AAMI/ISO 13408-5:2006. 14-352 Aseptic processing of health care products—Part 6: Isolator systems ANSI/AAMI/ISO 13408-6:2005. 14-353 Sterilization of health care products—Chemical indicators—Part 1: General requirements ISO 11140-1 Second edition 2005-07-15. 14-354 Sterilization of health care products—Biological and chemical indicators—Test equipment ISO 18472 First edition 2006-06-01. 14-355 Packaging for terminally sterilized medical devices—Part 1: Requirements for materials, sterile barrier systems and packaging systems ISO 11607-1 First edition 2006-04-15. 14-356 Packaging for terminally sterilized medical devices—Part 2: Validation requirements for forming, sealing and assembly processes ISO 11607-2 First edition 2006-04-15. 14-357 Sterilization of medical devices—Microbiological methods—Part 1: Determination of a population of microorganisms on products ISO 11737-1:2006 TECHNICAL CORRIGENDUM 1 Published 2007-05-15. M. Tissue Engineering 15-32 Standard Test Method for Determining Degree of Deacetylation in Chitosan Salts by Proton Nuclear Magnetic Resonance ( 1 H NMR) Spectroscopy ASTM F2260-03 (Reapproved 2008). 15-33 Standard Test Method for Determining the Molar Mass of Chitosan and Chitosan Salts by Size Exclusion Chromatography with Multi-angle Light Scattering Detection (SEC-MALS) ASTM F2602-08 1 . 15-34 Standard Test Method for Determining the Molar Mass of Sodium Alginate by Size Exclusion Chromatography with Multi-angle Light Scattering Detection (SEC-MALS) ASTM F2605-08 1 . 15-35 Standard Guide for Characterization of Hydrogels used in Regenerative Medicine ASTM F2900-11. 15-36 Standard Guide for Assessment of Adventitious Agents in Tissue Engineered Medical Products (TEMPs) ASTM F2383-11. 1 All standard titles in this table conform to the style requirements of the respective organizations. IV. List of Recognized Standards FDA maintains the Agency's current list of FDA recognized consensus standards in a searchable database that may be accessed directly at FDA's Internet site at http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfStandards/search.cfm. FDA will incorporate the modifications and minor revisions described in this notice into the database and, upon publication in the Federal Register , this recognition of consensus standards will be effective. FDA will announce additional modifications and minor revisions to the list of recognized consensus standards, as needed, in the Federal Register once a year, or more often, if necessary. V. Recommendation of Standards for Recognition by FDA Any person may recommend consensus standards as candidates for recognition under the new provision of section 514 of the FD&C Act by submitting such recommendations, with reasons for the recommendation, to the contact person (see FOR FURTHER INFORMATION CONTACT ). To be properly considered, such recommendations should contain, at a minimum, the following information: (1) Title of the standard; (2) any reference number and date; (3) name and address of the national or international standards development organization; (4) a proposed list of devices for which a declaration of conformity to this standard should routinely apply; and (5) a brief identification of the testing or performance or other characteristics of the device(s) that would be addressed by a declaration of conformity. VI. Electronic Access You may obtain a copy of “Guidance on the Recognition and Use of Consensus Standards” by using the Internet. CDRH maintains a site on the Internet for easy access to information including text, graphics, and files that you may download to a personal computer with access to the Internet. Updated on a regular basis, the CDRH home page includes the guidance as well as the current list of recognized standards and other standards-related documents. After publication in the Federal Register , this notice announcing “Modification to the List of Recognized Standards, Recognition List Number: 028'' will be available on the CDRH home page. You may access the CDRH home page at http://www.fda.gov/MedicalDevices. You may access “Guidance on the Recognition and Use of Consensus Standards,” and the searchable database for “FDA Recognized Consensus Standards” at http://www.fda.gov/MedicalDevices/DeviceRegulationandGuidance/Standards. This Federal Register document on modifications in FDA's recognition of consensus standards is available at http://www.fda.gov/MedicalDevices/DeviceRegulationandGuidance/Standards/ucm123792.htm. VII. Submission of Comments and Effective Date Interested persons may submit to the contact person (see FOR FURTHER INFORMATION CONTACT ) either electronic or written comments regarding this document. It is only necessary to send one set of comments. Identify comments with the docket number found in brackets in the heading of this document. FDA will consider any comments received in determining whether to amend the current listing of modifications to the list of recognized standards, Recognition List Number: 028. These modifications to the list or recognized standards are effective upon publication of this notice in the Federal Register . Dated: March 12, 2012. Leslie Kux, Acting Assistant Commissioner for Policy. [FR Doc. 2012-6389 Filed 3-15-12; 8:45 am] BILLING CODE 4160-01-P --- Source: Frix Law Library, https://www.frixlaw.com/law-library/documents/fr%3A2012-6389. Public record. Not legal advice.