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

    FISHER DIAGNOSTICS KDA CALIBRATOR II

    K Number: K851151 · Decision May 20, 1985
    View on FDA
    Classifications
    1
    FEI Numbers
    101
    Registration Numbers
    101
    Same Product Code
    301
    Applicant Total
    89
    Review Days
    60

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    Basic Information

    Device Name
    FISHER DIAGNOSTICS KDA CALIBRATOR II
    K Number
    K851151
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.1150
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Applicant
    Fisher Scientific Co., LLC
    Date Received
    March 21, 1985
    Decision Date
    May 20, 1985
    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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