21 CFR 864, Subpart I - Hematology Reagents
- § 864.8100 — Bothrops atrox reagent.
- § 864.8150 — Calibrator for cell indices.
- § 864.8165 — Calibrator for hemoglobin or hematocrit measurement.
- § 864.8175 — Calibrator for platelet counting.
- § 864.8185 — Calibrator for red cell and white cell counting.
- § 864.8200 — Blood cell diluent.
- § 864.8500 — Lymphocyte separation medium.
- § 864.8540 — Red cell lysing reagent.
- § 864.8625 — Hematology quality control mixture.
- § 864.8950 — Russell viper venom reagent.
Title 21 published on 2012-04-01
The following are only the Rules published in the Federal Register after the published date of Title 21.
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§ 360c - Classification of devices intended for human use
§ 360e - Premarket approval
§ 360j - General provisions respecting control of devices intended for human use
Title 21 published on 2012-04-01
The following are ALL rules, proposed rules, and notices (chronologically) published in the Federal Register relating to 21 CFR 864 after this date.
GPO FDSys XML | Text type regulations.gov FR Doc. 2013-06826 RIN Docket No. FDA-2013-N-0011 DEPARTMENT OF HEALTH AND HUMAN SERVICES, Food and Drug Administration Final rule; technical amendment. This rule is effective March 26, 2013. 21 CFR Parts 814, 822, 862, 864, 866, 868, 870, 872, 874, 876, 878, 880, 882, 884, 886, 888, 890, and 892 The Food and Drug Administration (FDA) is amending certain medical device regulations to correct minor errors in the Code of Federal Regulations (CFR). This action is editorial in nature and is intended to provide accuracy and clarity to the Agency's regulations.