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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 C - Postmarket Surveillance Plan |
| § 822.8 - When, where, and how must I submit my postmarket surveillance plan? |
| § 822.9 - What must I include in my submission? |
| § 822.10 - What must I include in my surveillance plan? |
| § 822.11 - What should I consider when designing my plan to conduct postmarket surveillance? |
| § 822.12 - Do you have any information that will help me prepare my submission or design my postmarket surveillance plan? |
| § 822.13 - [Reserved] |
| § 822.14 - May I reference information previously submitted instead of submitting it again? |
| § 822.15 - How long must I conduct postmarket surveillance of my device? |