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

    T4 NO SPIN(TM) COATED TUBE RADIOIMMUNOASSAY KIT

    K Number: K870573 · Decision Apr 22, 1987
    View on FDA
    Classifications
    1
    FEI Numbers
    13
    Registration Numbers
    13
    Same Product Code
    120
    Applicant Total
    14
    Review Days
    71

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    Basic Information

    Device Name
    T4 NO SPIN(TM) COATED TUBE RADIOIMMUNOASSAY KIT
    K Number
    K870573
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.1700
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Applicant
    Cambridge Medical Technology
    Date Received
    February 10, 1987
    Decision Date
    April 22, 1987
    Product Code
    CDX
    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
    CDX Radioimmunoassay, Total Thyroxine

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