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

    LASERMED OCULASE ARGON LASER

    K Number: K828583 · Decision Jan 14, 1983
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    3
    Review Days
    52

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    Basic Information

    Device Name
    LASERMED OCULASE ARGON LASER
    K Number
    K828583
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Lasermed Corp.
    Date Received
    November 23, 1982
    Decision Date
    January 14, 1983
    Advisory Committee
    Unknown
    Review Advisory Committee
    RA
    Third Party
    N

    Other Clearances by Lasermed Corp.

    K Number Device Name
    K843594 AIRVIT MODEL 8500
    K833532 OCULASE 514 OPHTHALMIC ARGON LASER