BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Stimulator, Functional Walking Neuromuscular, Non-Invasive

    PMA: P900038 · Decision Apr 20, 1994
    View on FDA
    Classifications
    1
    FEI Numbers
    0
    Registration Numbers
    0

    Basic Information

    Device Name
    Stimulator, Functional Walking Neuromuscular, Non-Invasive
    Trade Name
    PARASTEP-I
    PMA Number
    P900038
    Device Class
    FDA Class 3
    Product Code
    MKD
    Generic Name
    Stimulator, functional walking neuromuscular, non-invasive
    Medical Specialty
    Unknown
    Advisory Committee
    Neurology
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    April 20, 1994
    Date Received
    May 21, 1990
    Expedited Review
    N
    Docket Number
    94M-0180

    Classifications

    This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    MKD Stimulator, Functional Walking Neuromuscular, Non-Invasive