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    FDA 510(k) FDA class 1 Substantially Equivalent 🇯🇵 Japan

    TRIMOTION INJECTOR

    K Number: K102999 · Decision Dec 29, 2011
    View on FDA
    Classifications
    1
    FEI Numbers
    5
    Registration Numbers
    5
    Same Product Code
    4
    Applicant Total
    1
    Review Days
    447

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    Basic Information

    Device Name
    TRIMOTION INJECTOR
    K Number
    K102999
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    886.4300
    Medical Specialty
    Ophthalmic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Kaneka Corp.
    Date Received
    October 8, 2010
    Decision Date
    December 29, 2011
    Product Code
    OTZ
    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
    OTZ Graft Insertion Instrument For Endothelial Keratoplasty

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