BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    IOL IMPLANTATION FORCEPS

    K Number: K883197 · Decision Aug 22, 1988
    View on FDA
    Classifications
    1
    FEI Numbers
    275
    Registration Numbers
    276
    Same Product Code
    43
    Applicant Total
    1
    Review Days
    25

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    Basic Information

    Device Name
    IOL IMPLANTATION FORCEPS
    K Number
    K883197
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    886.4350
    Medical Specialty
    Ophthalmic
    Decision
    Substantially Equivalent
    Applicant
    D & D Surgical
    Date Received
    July 28, 1988
    Decision Date
    August 22, 1988
    Product Code
    HNR
    Advisory Committee
    Ophthalmic
    Review Advisory Committee
    OP
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    HNR Forceps, Ophthalmic

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