21 CFR 862, Subpart C - Clinical Laboratory Instruments
- § 862.2050 — General purpose laboratory equipment labeled or promoted for a specific medical use.
- § 862.2100 — Calculator/data processing module for clinical use.
- § 862.2140 — Centrifugal chemistry analyzer for clinical use.
- § 862.2150 — Continuous flow sequential multiple chemistry analyzer for clinical use.
- § 862.2160 — Discrete photometric chemistry analyzer for clinical use.
- § 862.2170 — Micro chemistry analyzer for clinical use.
- § 862.2230 — Chromatographic separation material for clinical use.
- § 862.2250 — Gas liquid chromatography system for clinical use.
- § 862.2260 — High pressure liquid chromatography system for clinical use.
- § 862.2270 — Thin-layer chromatography system for clinical use.
- § 862.2300 — Colorimeter, photometer, or spectrophotometer for clinical use.
- § 862.2310 — Clinical sample concentrator.
- § 862.2320 — Beta or gamma counter for clinical use.
- § 862.2400 — Densitometer/scanner (integrating, reflectance, TLC, or radiochromatogram) for clinical use.
- § 862.2485 — Electrophoresis apparatus for clinical use.
- § 862.2500 — Enzyme analyzer for clinical use.
- § 862.2540 — Flame emission photometer for clinical use.
- § 862.2560 — Fluorometer for clinical use.
- § 862.2570 — Instrumentation for clinical multiplex test systems.
- § 862.2680 — Microtitrator for clinical use.
- § 862.2700 — Nephelometer for clinical use.
- § 862.2720 — Plasma oncometer for clinical use.
- § 862.2730 — Osmometer for clinical use.
- § 862.2750 — Pipetting and diluting system for clinical use.
- § 862.2800 — Refractometer for clinical use.
- § 862.2850 — Atomic absorption spectrophotometer for clinical use.
- § 862.2860 — Mass spectrometer for clinical use.
- § 862.2900 — Automated urinalysis system.
- § 862.2920 — Plasma viscometer for clinical use.
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.
For a complete list of all Rules, Proposed Rules, and Notices view the Rulemaking tab.
This is a list of United States Code sections, Statutes at Large, Public Laws, and Presidential Documents, which provide rulemaking authority for this CFR Part.
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§ 360c - Classification of devices intended for human use
§ 360e - Premarket approval
§ 360i - Records and reports on devices
§ 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 862 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.