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Code of Federal Regulations (Last Updated: November 8, 2024) |
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Title 21 - Food and Drugs |
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Chapter I - Food and Drug Administration, Department of Health and Human Services |
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SubChapter H - Medical Devices |
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Part 822 - Postmarket Surveillance |
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Subpart E - Responsibilities of Manufacturers |
| § 822.24 - What are my responsibilities once I am notified that I am required to conduct postmarket surveillance? |
| § 822.25 - What are my responsibilities after my postmarket surveillance plan has been approved? |
| § 822.26 - If my company changes ownership, what must I do? |
| § 822.27 - If I go out of business, what must I do? |
| § 822.28 - If I stop marketing the device subject to postmarket surveillance, what must I do? |