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

    MODEL 900 PHOTOCOAGULATOR WITH GREEN-ONLY OPTIONS

    K Number: K827383 · Decision Nov 23, 1982
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    3
    Review Days
    25

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    Basic Information

    Device Name
    MODEL 900 PHOTOCOAGULATOR WITH GREEN-ONLY OPTIONS
    K Number
    K827383
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Coherent Radiation Laboratories
    Date Received
    October 29, 1982
    Decision Date
    November 23, 1982
    Advisory Committee
    Unknown
    Review Advisory Committee
    RA
    Third Party
    N

    Other Clearances by Coherent Radiation Laboratories

    K Number Device Name
    K837235 MODEL 920 ARGON LASER SYSTEM
    K837125 SYSTEM 900 TWO ROOM REMOTE FIBERS