21 CFR Part 803 - PART 803—MEDICAL DEVICE REPORTING
- Subpart A—General Provisions (§§ 803.1 - 803.19)
- Subpart B—Generally Applicable Requirements for Individual Adverse Event Reports (§§ 803.20 - 803.23)
- Subpart C—User Facility Reporting Requirements (§§ 803.30 - 803.33)
- Subpart D—Importer Reporting Requirements (§§ 803.40 - 803.42)
- Subpart E—Manufacturer Reporting Requirements (§§ 803.50 - 803.58)
The following state regulations pages link to this page.
Virginia