Postmarket Surveillance Plan

  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
  7. Postmarket Surveillance Plan

Checkout our iOS App for a better way to browser and research.

Section
822.8

When, where, and how must I submit my postmarket surveillance plan?

Section
822.9

What must I include in my submission?

Section
822.10

What must I include in my surveillance plan?

Section
822.11

What should I consider when designing my plan to conduct postmarket surveillance?

Section
822.12

Do you have any information that will help me prepare my submission or design my postmarket surveillance plan?

Section
822.13

§ 822.13 [Reserved]

Section
822.14

May I reference information previously submitted instead of submitting it again?

Section
822.15

How long must I conduct postmarket surveillance of my device?