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

    CONCENTRIC NEEDLE ELECTRODES-VARIOUS SIZES W/CONNE

    K Number: K850107 · Decision Apr 11, 1985
    View on FDA
    Classifications
    1
    FEI Numbers
    64
    Registration Numbers
    64
    Same Product Code
    52
    Applicant Total
    26
    Review Days
    91

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    Basic Information

    Device Name
    CONCENTRIC NEEDLE ELECTRODES-VARIOUS SIZES W/CONNE
    K Number
    K850107
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    882.1350
    Medical Specialty
    Neurology
    Decision
    Substantially Equivalent
    Applicant
    Nicolet Biomedical Instruments
    Date Received
    January 10, 1985
    Decision Date
    April 11, 1985
    Product Code
    GXZ
    Advisory Committee
    Neurology
    Review Advisory Committee
    NE
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    GXZ Electrode, Needle

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