Federal (United States) · Regulations
Part 803 — MEDICAL DEVICE REPORTING
26 sections
5 groups
- Subpart A — General Provisions12 sections
- Subpart B — Generally Applicable Requirements for Individual Adverse Event Reports4 sections
- Subpart C — User Facility Reporting Requirements3 sections
- Subpart D — Importer Reporting Requirements2 sections
- Subpart E — Manufacturer Reporting Requirements5 sections