BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    CARDIOFOCUS DIODE LASER SYSTEM, MODELS 60R, 60NR, 30NR

    K Number: K013201 · Decision Mar 18, 2002
    View on FDA
    Classifications
    1
    FEI Numbers
    476
    Registration Numbers
    479
    Same Product Code
    2793
    Applicant Total
    5
    Review Days
    174

    Basic Information

    Device Name
    CARDIOFOCUS DIODE LASER SYSTEM, MODELS 60R, 60NR, 30NR
    K Number
    K013201
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4810
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    CARDIOFOCUS, INC.
    Date Received
    September 25, 2001
    Decision Date
    March 18, 2002
    Product Code
    GEX
    Advisory Committee
    General, Plastic Surgery
    Review Advisory Committee
    SU
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    GEX Powered Laser Surgical Instrument

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