21 C.F.R. § 866.5700

Whole human plasma or serum immunological test system.

Last amended: 2016Year: 2026Length: 116 wordsSubsections: 1Official source

Cite as 21 C.F.R. § 866.5700 (2026)

(a) Identification. A whole human plasma or serum immunological test system is a device that consists of reagents used to measure by immunochemical techniques the proteins in plasma or serum. Measurements of proteins in plasma or serum aid in the diagnosis of any disease concerned with abnormal levels of plasma or serum proteins, e.g., agammaglobulinemia, allergies, multiple myeloma, rheumatoid vasculitis, or hereditary angioneurotic edema. (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 § 866.9. [47 FR 50823, Nov. 9, 1982, as amended at 59 FR 63007, Dec. 7, 1994; 66 FR 38793, July 25, 2001]
Cross-references to the CFR
866.9.
21 C.F.R. § 866.5700: Whole human plasma or serum immunological test system. | Justis AI