Postmarket Surveillance

  1. Law
  2. CFR 21
  3. Food and Drugs
  4. Food and Drug Administration, Department of Health and Human Services
  5. Medical Devices
  6. Postmarket Surveillance

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Subpart
A

General Provisions

Subpart
B

Notification

Subpart
C

Postmarket Surveillance Plan

Subpart
D

FDA Review and Action

Subpart
E

Responsibilities of Manufacturers

Subpart
F

Waivers and Exemptions

Subpart
G

Records and Reports