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

    OFTALMOGRAF

    K Number: K833024 · Decision Apr 26, 1984
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    2
    Review Days
    233

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    Basic Information

    Device Name
    OFTALMOGRAF
    K Number
    K833024
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Universal Instruments Corp.
    Date Received
    September 6, 1983
    Decision Date
    April 26, 1984
    Advisory Committee
    Unknown
    Review Advisory Committee
    OP
    Third Party
    N

    Other Clearances by Universal Instruments Corp.

    K Number Device Name
    K770193 PIPETTOR, 400, CENTRIFICHEM SYSTEM