BEUDAMED
    FDA PMA FDA Class 3 30-Day Notice Accepted 🇺🇸 United States

    Stimulator, Fetal, Acoustic

    PMA: P870025 · Supplement: S010 · Decision Oct 12, 2011
    View on FDA
    Classifications
    1
    FEI Numbers
    0
    Registration Numbers
    0

    Basic Information

    Device Name
    Stimulator, Fetal, Acoustic
    Trade Name
    FETAL ACOUSTIC STIMULATOR
    PMA Number
    P870025
    Supplement Number
    S010
    Device Class
    FDA Class 3
    Product Code
    MCP
    Generic Name
    Stimulator, fetal, acoustic
    Medical Specialty
    Unknown
    Advisory Committee
    Obstetrics/Gynecology
    Decision
    30-Day Notice Accepted
    Decision Code
    OK30
    Decision Date
    October 12, 2011
    Date Received
    September 12, 2011
    Supplement Type
    30-Day Notice
    Supplement Reason
    Process Change - Manufacturer/Sterilizer/Packager/Supplier
    Expedited Review
    N

    Advisory Committee Statement

    CHANGES TO THE SUPPLIERS FOR COMPONENTS OF THE FAST DEVICE.

    Classifications

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

    Product Code Device Name
    MCP Stimulator, Fetal, Acoustic