BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter

    PMA: P010068 · Supplement: S002 · Decision Jan 14, 2004
    View on FDA
    Classifications
    1
    FEI Numbers
    46
    Registration Numbers
    46

    Basic Information

    Device Name
    Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter
    Trade Name
    QWIKSTAR DS DIAGNOSTIC/ABLATION CATHETER
    PMA Number
    P010068
    Supplement Number
    S002
    Device Class
    FDA Class 3
    Product Code
    OAD
    Generic Name
    catheter, percutaneous, cardiac ablation, for treatment of atrial flutter
    Medical Specialty
    Unknown
    Advisory Committee
    Cardiovascular
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    January 14, 2004
    Date Received
    November 3, 2003
    Supplement Type
    Real-Time Process
    Supplement Reason
    Change Design/Components/Specifications/Material
    Expedited Review
    N

    Advisory Committee Statement

    APPROVAL FOR MODIFICATIONS MAD TO THE NAVISTAR DS 8MM TIP DEFLECTABLE DIAGNOSTIC/ABLATION CATHETER APPROVED UNDER P010068 AND THE QWIKSTAR 4 MM DEFLECTABLE TIP DIAGNOSTIC/ABLATION CATHETER APPROVED UNDER P990025/S004. THE DEVICE, AS MODIFIED, WILL BE MARKETED UNDER THE TRADE NAME QWIKSTAR DS DIAGNOSTIC/ABLATION CATHETER AND IS INDICATED FOR CATHETER BASED CARDIAC ELECTROPHYSIOLOGICAL MAPPING (STIMULATION AND RECORDING) AND WHEN USED WITH THE STOCKERT 70 RF GENERATOR (SOFTWARE VERSION 1.033 OR HIGHER) FOR THE TREATMENT OF TYPE I ATRIAL FLUTTER IN PATIENTS 18 YEARS OR OLDER.

    Classifications

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

    Product Code Device Name
    OAD Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter