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

    MODEL 920 ARGON LASER SYSTEM

    K Number: K837235 · Decision Apr 4, 1983
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    3
    Review Days
    34

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    Basic Information

    Device Name
    MODEL 920 ARGON LASER SYSTEM
    K Number
    K837235
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Coherent Radiation Laboratories
    Date Received
    March 1, 1983
    Decision Date
    April 4, 1983
    Advisory Committee
    Unknown
    Review Advisory Committee
    RA
    Third Party
    N

    Other Clearances by Coherent Radiation Laboratories

    K Number Device Name
    K837125 SYSTEM 900 TWO ROOM REMOTE FIBERS
    K827383 MODEL 900 PHOTOCOAGULATOR WITH GREEN-ONLY OPTIONS