PART 803—MEDICAL DEVICE REPORTING
- SUBPART A—General Provisions (§803.1 to §803.19)
- SUBPART B—Generally Applicable Requirements for Individual Adverse Event Reports (§803.20 to §803.22)
- SUBPART C—User Facility Reporting Requirements (§803.30 to §803.33)
- SUBPART D—Importer Reporting Requirements (§803.40 to §803.42)
- SUBPART E—Manufacturer Reporting Requirements (§803.50 to §803.58)