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

    EX-308 EXCIMER LASER FOR PHOTOTHERAPY TREATMENT OF VITILIGO

    K Number: K020973 · Decision Mar 29, 2002
    View on FDA
    Classifications
    1
    FEI Numbers
    476
    Registration Numbers
    479
    Same Product Code
    2793
    Applicant Total
    2
    Review Days
    3

    Basic Information

    Device Name
    EX-308 EXCIMER LASER FOR PHOTOTHERAPY TREATMENT OF VITILIGO
    K Number
    K020973
    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
    SURGILIGHT, INC.
    Date Received
    March 26, 2002
    Decision Date
    March 29, 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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    Other Clearances by SURGILIGHT, INC.

    K Number Device Name
    K993328 SURGILIGHT, INC EXCIMER LASER