BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Implantable Pacemaker Pulse-Generator

    PMA: P910020 · Supplement: S012 · Decision Jul 31, 1996
    View on FDA
    Classifications
    1
    FEI Numbers
    28
    Registration Numbers
    28

    Basic Information

    Device Name
    Implantable Pacemaker Pulse-Generator
    Trade Name
    UNITY MODEL 292-06 SINGLE PASS PULSE GENERATOR
    PMA Number
    P910020
    Supplement Number
    S012
    Device Class
    FDA Class 3
    Product Code
    DXY
    Generic Name
    implantable pacemaker Pulse-generator
    Regulation Number
    870.3610
    Medical Specialty
    Cardiovascular
    Advisory Committee
    Cardiovascular
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    July 31, 1996
    Date Received
    September 11, 1995
    Supplement Type
    Normal 180 Day Track
    Supplement Reason
    Change Design/Components/Specifications/Material
    Expedited Review
    N

    Advisory Committee Statement

    APPROVAL FOR THE UNITY MODEL 292-07 SINGLE PASS (VDDR) PULSE GENERATOR WITH UNIPASS LEADS MODELS 425-02, 425-04 AND 425-06 AND MODEL 531-60 GRAPHICS PROGRAM MODULE. THE DEVICE, AS MODIFIED, WILL BE MARKETED UNDER THE TRADE NAME UNITY

    Classifications

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

    Product Code Device Name
    DXY Implantable Pacemaker Pulse-Generator