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Federal regulations · Through 2026-08-25 · Newer source version available

21 CFR 862.2260: High pressure liquid chromatography system for clinical use.

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Where this section sits in the code
  1. Title 21—Food and Drugs
  2. CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
  3. SUBCHAPTER H—MEDICAL DEVICES
  4. PART 862—CLINICAL CHEMISTRY AND CLINICAL TOXICOLOGY DEVICES
  5. Subpart C—Clinical Laboratory Instruments

(a) Identification. A high pressure liquid chromatography system for clinical use is a device intended to separate one or more drugs or compounds from a solution by processing the mixture of compounds (solutes) through a column packed with materials of uniform size (stationary phase) under the influence of a high pressure liquid (mobile phase). Separation of the solutes occurs either by absorption, sieving, partition, or selective affinity.

(b) Classification. Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to § 862.9.

Collected 2026-08-27T02:24:47Z. Source file · JSON

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