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

    INTRALASE FS LASER

    K Number: K041893 · Decision Jul 29, 2005
    View on FDA
    Classifications
    1
    FEI Numbers
    476
    Registration Numbers
    479
    Same Product Code
    2793
    Applicant Total
    8
    Review Days
    381

    Basic Information

    Device Name
    INTRALASE FS LASER
    K Number
    K041893
    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
    INTRALASE CORP.
    Date Received
    July 13, 2004
    Decision Date
    July 29, 2005
    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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    Other Clearances by INTRALASE CORP.

    K Number Device Name
    K073404 IFS LASER SYSTEM
    K063682 INTRALASE FUSION LASER
    K031960 INTRALASE FS LASER
    K013941 PULSION FS LASER KERATOME
    K002890 INTRALASE 600C LASER KERATOME
    K001211 MODIFICATION TO INTRALASE 600C LASER KERATOME
    K993153 INTRALASE 600C LASER KERATOME