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

    NERVEL-NERVE CONDUCTION VELOCITY METER

    K Number: K760689 · Decision Oct 5, 1976
    View on FDA
    Classifications
    1
    FEI Numbers
    27
    Registration Numbers
    27
    Same Product Code
    26
    Applicant Total
    1
    Review Days
    14

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    Basic Information

    Device Name
    NERVEL-NERVE CONDUCTION VELOCITY METER
    K Number
    K760689
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    882.1550
    Medical Specialty
    Neurology
    Decision
    Substantially Equivalent
    Applicant
    Bak Electronics
    Date Received
    September 21, 1976
    Decision Date
    October 5, 1976
    Product Code
    JXE
    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
    JXE Device, Nerve Conduction Velocity Measurement

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