BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Permanent Pacemaker Electrode

    PMA: P950037 · Supplement: S041 · Decision Dec 21, 2005
    View on FDA
    Classifications
    1
    FEI Numbers
    24
    Registration Numbers
    24

    Basic Information

    Device Name
    Permanent Pacemaker Electrode
    Trade Name
    CYLOS FAMILY OF PULSE GENERATORS
    PMA Number
    P950037
    Supplement Number
    S041
    Device Class
    FDA Class 3
    Product Code
    DTB
    Generic Name
    permanent pacemaker Electrode
    Regulation Number
    870.3680
    Medical Specialty
    Cardiovascular
    Advisory Committee
    Cardiovascular
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    December 21, 2005
    Date Received
    September 26, 2005
    Supplement Type
    Real-Time Process
    Supplement Reason
    Change Design/Components/Specifications/Material
    Expedited Review
    N

    Advisory Committee Statement

    APPROVAL FOR THE CYLOS DR/DR-T AND CYLOS VR PULSE GENERATORS AND THE A-K00.6.U PROGRAMMER SOFTWARE (FOR USE WITH THE EPR 1000PLUS AND TMS 1000 PLUS PROGRAMMERS); THE 504.U PROGRAMMER SOFTWARE (FOR USE WITH THE ICS 3000 PROGRAMMER; AND THE HOME MONITORING SERVICE CENTER II VERSION 1.8.0.

    Classifications

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

    Product Code Device Name
    DTB Permanent Pacemaker Electrode