Part 803 — Medical Device Reporting
- Subpt. A General Provisions §§803.1 to 803.19
- Subpt. B Generally Applicable Requirements for Individual Adverse Event Reports §§803.20 to 803.23
- Subpt. C User Facility Reporting Requirements §§803.30 to 803.33
- Subpt. D Importer Reporting Requirements §§803.40 to 803.42
- Subpt. E Manufacturer Reporting Requirements §§803.50 to 803.58