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

21 CFR 862.1075: Androstenedione 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. An androstenedione test system is a device intended to measure androstenedione (a substance secreted by the testes, ovary, and adrenal glands) in serum. Adrostenedione measurements are used in the diagnosis and treatment of females with excessive levels of androgen (male sex hormone) production.

(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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