Subpart A. Subpart A—General Provisions

• § 803.1 - What does this part cover?
• § 803.3 - How does FDA define the terms used in this part?
• § 803.9 - What information from the reports do we disclose to the public?
• § 803.10 - Generally, what are the reporting requirements that apply to me?
• § 803.11 - What form should I use to submit reports of individual adverse events and where do I obtain these forms?
• § 803.12 - How do I submit initial and supplemental or followup reports?
• § 803.13 - Do I need to submit reports in English?
• § 803.15 - How will I know if you require more information about my medical device report?
• § 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?
• § 803.17 - What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?
• § 803.18 - What are the requirements for establishing and maintaining MDR files or records that apply to me?
• § 803.19 - Are there exemptions, variances, or alternative forms of adverse event reporting requirements?