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

    NERVE STIMULATOR, DIGITAL PERIPHERAL

    K Number: K791047 · Decision Jun 13, 1979
    View on FDA
    Classifications
    1
    FEI Numbers
    19
    Registration Numbers
    19
    Same Product Code
    62
    Applicant Total
    645
    Review Days
    7

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    Basic Information

    Device Name
    NERVE STIMULATOR, DIGITAL PERIPHERAL
    K Number
    K791047
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.2775
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Applicant
    C.R. Bard, Inc.
    Date Received
    June 6, 1979
    Decision Date
    June 13, 1979
    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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