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

    COHERENT SYSTEM 920 ARGON/DYE PHOTOCOAGULATOR

    K Number: K882160 · Decision Jun 22, 1988
    View on FDA
    Classifications
    1
    FEI Numbers
    476
    Registration Numbers
    479
    Same Product Code
    2793
    Applicant Total
    2
    Review Days
    30

    Basic Information

    Device Name
    COHERENT SYSTEM 920 ARGON/DYE PHOTOCOAGULATOR
    K Number
    K882160
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4810
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    COHERENT MEDICAL LASERS
    Date Received
    May 23, 1988
    Decision Date
    June 22, 1988
    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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