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