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

    EMG NAVIGATOR & EMG TRAVELER

    K Number: K893130 · Decision Mar 20, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    70
    Registration Numbers
    70
    Same Product Code
    74
    Applicant Total
    45
    Review Days
    329

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    Basic Information

    Device Name
    EMG NAVIGATOR & EMG TRAVELER
    K Number
    K893130
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    890.1375
    Medical Specialty
    Physical Medicine
    Decision
    Substantially Equivalent
    Applicant
    Bio-Logic Systems Corp.
    Date Received
    April 25, 1989
    Decision Date
    March 20, 1990
    Product Code
    IKN
    Advisory Committee
    Physical Medicine
    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
    IKN Electromyograph, Diagnostic

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