Title 21
PART 610 SUBPART E
Subpart E - Testing Requirements for Relevant Transfusion-Transmitted Infections
- 21 U.S.C. 321, 331, 351, 352, 353, 355, 360, 360c, 360d, 360h, 360i, 371, 372, 374, 381; 42 U.S.C. 216, 262, 263, 263a, 264.
- 38 FR 32056, Nov. 20, 1973, unless otherwise noted.
21:7.0.1.1.5.5.1.1 | SECTION 610.39 | 610.39 Definitions. | |
21:7.0.1.1.5.5.1.2 | SECTION 610.40 | 610.40 Test requirements. | |
21:7.0.1.1.5.5.1.3 | SECTION 610.41 | 610.41 Donor deferral. | |
21:7.0.1.1.5.5.1.4 | SECTION 610.42 | 610.42 Restrictions on use for further manufacture of medical devices. | |
21:7.0.1.1.5.5.1.5 | SECTION 610.44 | 610.44 Use of reference panels by manufacturers of test kits. | |
21:7.0.1.1.5.5.1.6 | SECTION 610.46 | 610.46 Human immunodeficiency virus (HIV) “lookback” requirements. | |
21:7.0.1.1.5.5.1.7 | SECTION 610.47 | 610.47 Hepatitis C virus (HCV) “lookback” requirements. | |
21:7.0.1.1.5.5.1.8 | SECTION 610.48 | 610.48 [Reserved] |