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

    BAYER SPECIFIC PROTEIN REFERENCE SERUM

    K Number: K033791 · Decision Feb 13, 2004
    View on FDA
    Classifications
    1
    FEI Numbers
    107
    Registration Numbers
    107
    Same Product Code
    301
    Applicant Total
    41
    Review Days
    71

    Basic Information

    Device Name
    BAYER SPECIFIC PROTEIN REFERENCE SERUM
    K Number
    K033791
    Device Class
    FDA class 2
    Clearance Type
    Abbreviated
    Regulation Number
    862.1150
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    BAYER HEALTHCARE, LLC
    Date Received
    December 4, 2003
    Decision Date
    February 13, 2004
    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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