21 CFR Part 803 - MEDICAL DEVICE REPORTING; (Eff. Until 8-14-15)
- 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)
Link to an amendment published at 79 FR 8846, Feb. 14, 2014.
Source:
70 FR 9519, July 13, 2005, unless otherwise noted
Effective Date Note:
At 79 FR 8846, Feb. 14, 2014, part 803 was revised, effective Aug. 14, 2015. For the convenience of the user, the revised text appears after this part.
Title 21 published on 2015-04-01.
No entries appear in the Federal Register after this date, for 21 CFR Part 803.