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

    RETRACTIVE INCISION MICROMETER (RIM) GUAGE

    K Number: K882402 · Decision Aug 22, 1988
    View on FDA
    Classifications
    1
    FEI Numbers
    206
    Registration Numbers
    207
    Same Product Code
    53
    Applicant Total
    1
    Review Days
    73

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    Basic Information

    Device Name
    RETRACTIVE INCISION MICROMETER (RIM) GUAGE
    K Number
    K882402
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    886.4350
    Medical Specialty
    Ophthalmic
    Decision
    Substantially Equivalent
    Applicant
    Optical Center
    Date Received
    June 10, 1988
    Decision Date
    August 22, 1988
    Product Code
    HNN
    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
    HNN Knife, Ophthalmic

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