21 C.F.R. · Food and Drugs
21 C.F.R. § 866.4540

Immunonephelometer equipment.

Title 21 C.F.R. ● ACTIVE Primary Source
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21 C.F.R. § 866.4540 — Immunonephelometer equipment.

§ 866.4540 Immunonephelometer equipment. (a) Identification. Immunonephelometer equipment for clinical use with its electrical power supply is a device that measures light scattering from antigen-antibody complexes. The concentration of these complexes may be measured by means of reflected light. A beam of light passed through a solution is scattered by the particles in suspension. The amount of light is detected by a photodetector, which converts light energy into electrical energy. The amount of electrical energy registers on a readout system such as a digital voltmeter or a recording chart. This electrical readout is called the light-scattering value and is used to measure the concentration of antigen-antibody complexes. This generic type of device includes devices with various kinds of light sources, such as laser equipment. (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 54 FR 25047, June 12, 1989; 66 FR 38792, July 25, 2001]

Source: ecfr.gov · govinfo.gov — public domain Official Source ↗
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The regulatory text of 21 C.F.R. § 866.4540 is reproduced from the official Code of Federal Regulations as published by the Office of the Federal Register and the National Archives and Records Administration.
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