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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 B - Notification |
| § 822.5 - How will I know if I must conduct postmarket surveillance? |
| § 822.6 - When will you notify me that I am required to conduct postmarket surveillance? |
| § 822.7 - What should I do if I do not agree that postmarket surveillance is appropriate? |