BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇳🇿 New Zealand

    MODEL NS242 CONSTANT CURRENT PERIPHERAL NERVE STIM

    K Number: K883868 · Decision Nov 28, 1988
    View on FDA
    Classifications
    1
    FEI Numbers
    19
    Registration Numbers
    19
    Same Product Code
    62
    Applicant Total
    17
    Review Days
    76

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    Basic Information

    Device Name
    MODEL NS242 CONSTANT CURRENT PERIPHERAL NERVE STIM
    K Number
    K883868
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.2775
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Applicant
    Fisher & Paykel Electronics , Ltd.
    Date Received
    September 13, 1988
    Decision Date
    November 28, 1988
    Product Code
    BXN
    Advisory Committee
    Anesthesiology
    Review Advisory Committee
    AN
    Third Party
    N

    Classifications

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

    Product Code Device Name
    BXN Stimulator, Nerve, Battery-Powered

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