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Responsibilities of Manufacturers
Law
CFR 21
Food and Drugs
Food and Drug Administration, Department of Health and Human Services
Medical Devices
Postmarket Surveillance
Responsibilities of Manufacturers
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Section
822.24
What are my responsibilities once I am notified that I am required to conduct postmarket surveillance?
Section
822.25
What are my responsibilities after my postmarket surveillance plan has been approved?
Section
822.26
If my company changes ownership, what must I do?
Section
822.27
If I go out of business, what must I do?
Section
822.28
If I stop marketing the device subject to postmarket surveillance, what must I do?