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

    INTRAOCULAR LENS

    K Number: K770728 · Decision Apr 28, 1977
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    2
    Review Days
    8

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    Basic Information

    Device Name
    INTRAOCULAR LENS
    K Number
    K770728
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Milton Roy Co. Analytical
    Date Received
    April 20, 1977
    Decision Date
    April 28, 1977
    Advisory Committee
    Unknown
    Review Advisory Committee
    OP
    Third Party
    N

    Other Clearances by Milton Roy Co. Analytical

    K Number Device Name
    K771065 DYLADE, MODEL DS