BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Device, Hemostasis, Vascular

    PMA: P920004 · Supplement: S016 · Decision Mar 7, 2002
    View on FDA
    Classifications
    1
    FEI Numbers
    33
    Registration Numbers
    33

    Basic Information

    Device Name
    Device, Hemostasis, Vascular
    Trade Name
    VASOSEAL VHD & ES DEVICES
    PMA Number
    P920004
    Supplement Number
    S016
    Device Class
    FDA Class 3
    Product Code
    MGB
    Generic Name
    Device, hemostasis, vascular
    Medical Specialty
    Unknown
    Advisory Committee
    Cardiovascular
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    March 7, 2002
    Date Received
    February 5, 2002
    Supplement Type
    Special (Immediate Track)
    Supplement Reason
    Labeling Change - Indications/instructions/shelf life/tradename
    Expedited Review
    N

    Advisory Committee Statement

    APPROVAL FOR A CHANGE IN THE INSTRUCTIONS FOR USE. SPECIFICALLY, TO REMOVE THE OCCLUSIVE PRESSURE WHILE MAINTAINING ADHESIVE (DEVICE) PLUNGER PRESSURE AND POSITIONS AFTER THE FIRST COLLAGEN CARTRIDGE HAS BEEN DEPLOYED.

    Classifications

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

    Product Code Device Name
    MGB Device, Hemostasis, Vascular