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

21 CFR 866.5510: Immunoglobulins A, G, M, D, and E immunological 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 866—IMMUNOLOGY AND MICROBIOLOGY DEVICES
  5. Subpart F—Immunological Test Systems

(a) Identification. An immunoglobulins A, G, M, D, and E immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the immunoglobulins A, G, M, D, an E (serum antibodies) in serum. Measurement of these immunoglobulins aids in the diagnosis of abnormal protein metabolism and the body's lack of ability to resist infectious agents.

(b) Classification. Class II (performance standards).

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

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