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

    OCULAR PRESSURE APPLICATOR

    K Number: K841652 · Decision Jun 1, 1984
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    3
    Review Days
    42

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    Basic Information

    Device Name
    OCULAR PRESSURE APPLICATOR
    K Number
    K841652
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    The Lebanon Corp.
    Date Received
    April 20, 1984
    Decision Date
    June 1, 1984
    Advisory Committee
    Unknown
    Review Advisory Committee
    OP
    Third Party
    N

    Other Clearances by The Lebanon Corp.

    K Number Device Name
    K821689 LEBANON MICROSCOPE
    K820526 RELIEF VALVE-HONAN INTRAOC. PRESSURE