21 CFR Part 822 - POSTMARKET SURVEILLANCE
- Subpart A - General Provisions (§§ 822.1 - 822.4)
- Subpart B - Notification (§§ 822.5 - 822.7)
- Subpart C - Postmarket Surveillance Plan (§§ 822.8 - 822.15)
- Subpart D - FDA Review and Action (§§ 822.16 - 822.23)
- Subpart E - Responsibilities of Manufacturers (§§ 822.24 - 822.28)
- Subpart F - Waivers and Exemptions (§§ 822.29 - 822.30)
- Subpart G - Records and Reports (§§ 822.31 - 822.38)