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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 - PART 809—IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USE
Subpart A [§ 809.3 - § 809.4] - Subpart A—General Provisions
Subpart B [§ 809.10 - § 809.11] - Subpart B—Labeling
Subpart C [§ 809.20 - § 809.40] - Subpart C—Requirements for Manufacturers and Producers
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