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Regulations last checked for updates: May 14, 2025

Title 21 - Food and Drugs last revised: May 12, 2025
All TitlesTitle 21Chapter IPart 660 - PART 660—ADDITIONAL STANDARDS FOR DIAGNOSTIC SUBSTANCES FOR LABORATORY TESTS
  • Subpart A [§ 660.1 - § 660.6] - Subpart A—Antibody to Hepatitis B Surface Antigen
  • Subpart B - Subpart B [Reserved]
  • Subpart C [§ 660.20 - § 660.28] - Subpart C—Blood Grouping Reagent
  • Subpart D [§ 660.30 - § 660.36] - Subpart D—Reagent Red Blood Cells
  • Subpart E [§ 660.40 - § 660.46] - Subpart E—Hepatitis B Surface Antigen
  • Subpart F [§ 660.50 - § 660.55] - Subpart F—Anti-Human Globulin
authority: 21 U.S.C. 321,331,351,352,353,355,360,360c,360d,360h,360i,371,372; 42 U.S.C. 216,262,263,263a,264
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