BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Device, Hemostasis, Vascular

    PMA: P010049 · Supplement: S008 · Decision Aug 13, 2003
    View on FDA
    Classifications
    1
    FEI Numbers
    33
    Registration Numbers
    33

    Basic Information

    Device Name
    Device, Hemostasis, Vascular
    Trade Name
    QUICKSEAL CONTROL ARTERIAL CLOSURE SYSTEM
    PMA Number
    P010049
    Supplement Number
    S008
    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
    August 13, 2003
    Date Received
    June 30, 2003
    Supplement Type
    Real-Time Process
    Supplement Reason
    Change Design/Components/Specifications/Material
    Expedited Review
    N

    Advisory Committee Statement

    APPROVAL TO MODIFY THE DEVICE TO REDUCE THE NUMBER OF PREPARATION STEPS, SIMPLIFY THE METHOD OF STAGING THE HEMOSTATIC SPONGE INTO DELIVERY CANNULA AND PROVIDE AN EASIER INTERFACE FOR FLUSHING THE DEPTH MARKER.

    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