Part 822 — Postmarket Surveillance

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• Subpt. A General Provisions §§822.1 to 822.4
• Subpt. B Notification §§822.5 to 822.7
• Subpt. C Postmarket Surveillance Plan §§822.8 to 822.15
• Subpt. D FDA Review and Action §§822.16 to 822.23
• Subpt. E Responsibilities of Manufacturers §§822.24 to 822.28
• Subpt. F Waivers and Exemptions §§822.29 to 822.30
• Subpt. G Records and Reports §§822.31 to 822.38