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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 809 - In Vitro Diagnostic Products for Human Use |
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Subpart B - Labeling |
| § 809.10 - Labeling for in vitro diagnostic products. |
| § 809.11 - Exceptions or alternatives to labeling requirements for in vitro diagnostic products for human use held by the Strategic National Stockpile. |