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

21 CFR 862.2500: Enzyme analyzer 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. An enzyme analyzer for clinical use is a device intended to measure enzymes in plasma or serum by nonkinetic or kinetic measurement of enzyme-catalyzed reactions. This device is used in conjunction with certain materials to measure a variety of enzymes as an aid in the diagnosis and treatment of certain enzyme-related disorders.

(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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