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US law
Federal (United States)
Regulations
Title 21 CFR — Food and Drugs
Chapter I
Part 822
Subpart E
Federal (United States) · Regulations
Subpart E
2 sections
2 sections
21 C.F.R. § 822.24
What are my responsibilities once I am notified that I am required to conduct postmarket surveillance?
21 C.F.R. § 822.28
If I stop marketing the device subject to postmarket surveillance, what must I do?
Subpart E | Federal (United States) Regulations | Justis AI