BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    CORTISOL RADIOIMMUNOASSAY KIT

    K Number: K832638 · Decision Sep 12, 1983
    View on FDA
    Classifications
    1
    FEI Numbers
    18
    Registration Numbers
    18
    Same Product Code
    83
    Applicant Total
    9
    Review Days
    39

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    Basic Information

    Device Name
    CORTISOL RADIOIMMUNOASSAY KIT
    K Number
    K832638
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.1205
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Applicant
    Bioclinical Group
    Date Received
    August 4, 1983
    Decision Date
    September 12, 1983
    Product Code
    CGR
    Advisory Committee
    Clinical Chemistry
    Review Advisory Committee
    CH
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    CGR Radioimmunoassay, Cortisol

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    K822515 B-HCG RADIOIMMUNOASSAY KIT
    K821241 FREE T4 RADIOIMMUNOASSAY KIT
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