21 C.F.R. · Food and Drugs
21 C.F.R. § 866.3520

Rubeola (measles) virus serological reagents.

Title 21 C.F.R. ● ACTIVE Primary Source
Regulatory Text

21 C.F.R. § 866.3520 — Rubeola (measles) virus serological reagents.

§ 866.3520 Rubeola (measles) virus serological reagents. (a) Identification. Rubeola (measles) virus serological reagents are devices that consist of antigens and antisera used in serological tests to identify antibodies to rubeola virus in serum. The identification aids in the diagnosis of measles and provides epidemiological information on the disease. Measles is an acute, highly infectious disease of the respiratory and reticuloendothelial tissues, particularly in children, characterized by a confluent and blotchy rash. (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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21 C.F.R. § 866.3520
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The regulatory text of 21 C.F.R. § 866.3520 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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