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

    CENTRIFICHEM COMB. SERUM-BASED CALIB.

    K Number: K802741 · Decision Dec 10, 1980
    View on FDA
    Classifications
    1
    FEI Numbers
    101
    Registration Numbers
    101
    Same Product Code
    301
    Applicant Total
    69
    Review Days
    37

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    Basic Information

    Device Name
    CENTRIFICHEM COMB. SERUM-BASED CALIB.
    K Number
    K802741
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.1150
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Applicant
    Union Carbide Corp.
    Date Received
    November 3, 1980
    Decision Date
    December 10, 1980
    Product Code
    JIX
    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
    JIX Calibrator, Multi-Analyte Mixture

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