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

21 CFR 862.1365: Glutathione test system.

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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 B—Clinical Chemistry Test Systems

(a) Identification. A glutathione test system is a device intended to measure glutathione (the tripeptide of glycine, cysteine, and glutamic acid) in erythrocytes (red blood cells). Glutathione measurements are used in the diagnosis and treatment of certain drug-induced hemolytic (erythrocyte destroying) anemias due to an inherited enzyme deficiency.

(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 the limitations in § 862.9

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

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