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U.S. Code of Federal Regulations
Regulations most recently checked for updates: Aug 28, 2025
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Title 21
Chapter I
Part 809
Subpart B - 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.
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