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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 F - Biologics |
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Part 607 - Establishment Registration and Product Listing for Manufacturers of Human Blood and Blood Products and Licensed Devices |
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Subpart E - Establishment Registration and Product Listing Of Licensed Devices |
| § 607.80 - Applicability of part 607 to licensed devices. |