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

    LASER PHOTOCOAGULATOR

    K Number: K827819 · Decision Jan 7, 1983
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    5
    Review Days
    80

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    Basic Information

    Device Name
    LASER PHOTOCOAGULATOR
    K Number
    K827819
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    American Laser Corp.
    Date Received
    October 19, 1982
    Decision Date
    January 7, 1983
    Advisory Committee
    Unknown
    Review Advisory Committee
    RA
    Third Party
    N

    Other Clearances by American Laser Corp.

    K Number Device Name
    K010046 NUVOLASE 532 MEDICAL LASER SYSTEM
    K990665 BQ/BM INTEGRATED LASER DELIVERY SYSTEM
    K990725 NUVOLASE 532 LASER SYSTEM
    K813429 LASER PHOTOCOAGULATOR ARGON MED. LASER