# 21 CFR § 803.13: Do I need to submit reports in English?

> Federal · Regulations · In force

URL: https://www.frixlaw.com/law-library/statutes/ecfr-21-803.13

## Section

- **Citation:** 21 CFR § 803.13
- **Heading:** Do I need to submit reports in English?
- **Jurisdiction:** Federal
- **Kind:** Regulations
- **Status:** In force
- **Text as of:** September 22, 2026
- **Source:** Publisher's official text
- **Location:** Title 21—Food and Drugs > CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES > SUBCHAPTER H—MEDICAL DEVICES > PART 803—MEDICAL DEVICE REPORTING > Subpart A—General Provisions

## Text

Yes. You must submit all reports required by this part in English.

## Nearby sections

- [21 CFR § 803.1 § 803.1 What does this part cover?](https://www.frixlaw.com/law-library/statutes/ecfr-21-803.1.md)
- [21 CFR § 803.3 § 803.3 How does FDA define the terms used in this part?](https://www.frixlaw.com/law-library/statutes/ecfr-21-803.3.md)
- [21 CFR § 803.9 § 803.9 What information from the reports do we disclose to the public?](https://www.frixlaw.com/law-library/statutes/ecfr-21-803.9.md)
- [21 CFR § 803.10 § 803.10 Generally, what are the reporting requirements that apply to me?](https://www.frixlaw.com/law-library/statutes/ecfr-21-803.10.md)
- [21 CFR § 803.11 § 803.11 What form should I use to submit reports of individual adverse events and where do I obtain these forms?](https://www.frixlaw.com/law-library/statutes/ecfr-21-803.11.md)
- [21 CFR § 803.12 § 803.12 How do I submit initial and supplemental or followup reports?](https://www.frixlaw.com/law-library/statutes/ecfr-21-803.12.md)
- [21 CFR § 803.13 § 803.13 Do I need to submit reports in English?](https://www.frixlaw.com/law-library/statutes/ecfr-21-803.13.md)
- [21 CFR § 803.15 § 803.15 How will I know if you require more information about my medical device report?](https://www.frixlaw.com/law-library/statutes/ecfr-21-803.15.md)
- [21 CFR § 803.16 § 803.16 When I submit a report, does the information in my report constitute an admission that the device caused or contributed to the reportable event?](https://www.frixlaw.com/law-library/statutes/ecfr-21-803.16.md)
- [21 CFR § 803.17 § 803.17 What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?](https://www.frixlaw.com/law-library/statutes/ecfr-21-803.17.md)
- [21 CFR § 803.18 § 803.18 What are the requirements for establishing and maintaining MDR files or records that apply to me?](https://www.frixlaw.com/law-library/statutes/ecfr-21-803.18.md)
- [21 CFR § 803.19 § 803.19 Are there exemptions, variances, or alternative forms of adverse event reporting requirements?](https://www.frixlaw.com/law-library/statutes/ecfr-21-803.19.md)
- [21 CFR § 803.20 § 803.20 How do I complete and submit an individual adverse event report?](https://www.frixlaw.com/law-library/statutes/ecfr-21-803.20.md)
- [21 CFR § 803.21 § 803.21 Where can I find the reporting codes for adverse events that I use with medical device reports?](https://www.frixlaw.com/law-library/statutes/ecfr-21-803.21.md)

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Source: Frix Law Library, https://www.frixlaw.com/law-library/statutes/ecfr-21-803.13. Check the current official text before relying on it. Not legal advice.