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

    TANDEM-MP OSTASE IMMUNOENZYMETRIC ASSAY

    K Number: K972666 · Decision Sep 11, 1997
    View on FDA
    Classifications
    1
    FEI Numbers
    8
    Registration Numbers
    8
    Same Product Code
    25
    Applicant Total
    63
    Review Days
    57

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    Basic Information

    Device Name
    TANDEM-MP OSTASE IMMUNOENZYMETRIC ASSAY
    K Number
    K972666
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.1050
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Hybritech, Inc.
    Date Received
    July 16, 1997
    Decision Date
    September 11, 1997
    Product Code
    CIN
    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
    CIN Electrophoretic Separation, Alkaline Phosphatase Isoenzymes

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