BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇦🇺 Australia

    LASEREX INTEGRE, MODEL LP2532

    K Number: K003955 · Decision Mar 15, 2001
    View on FDA
    Classifications
    1
    FEI Numbers
    478
    Registration Numbers
    480
    Same Product Code
    2867
    Applicant Total
    13
    Review Days
    84

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    Basic Information

    Device Name
    LASEREX INTEGRE, MODEL LP2532
    K Number
    K003955
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4810
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Ellex Medical Pty, Ltd.
    Date Received
    December 21, 2000
    Decision Date
    March 15, 2001
    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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