BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    Fujifilm Diathermic Slitter (FlushKnife), Diathermic Slitter (ClutchCutter)

    K Number: K151474 · Decision Feb 18, 2016
    View on FDA
    Classifications
    1
    FEI Numbers
    52
    Registration Numbers
    52
    Same Product Code
    45
    Applicant Total
    71
    Review Days
    262

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    Basic Information

    Device Name
    Fujifilm Diathermic Slitter (FlushKnife), Diathermic Slitter (ClutchCutter)
    K Number
    K151474
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.4300
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Fujifilm Medical System U.S.A., Inc.
    Date Received
    June 1, 2015
    Decision Date
    February 18, 2016
    Product Code
    KGE
    Advisory Committee
    Gastroenterology, Urology
    Review Advisory Committee
    GU
    Third Party
    N

    Classifications

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

    Product Code Device Name
    KGE Forceps, Biopsy, Electric

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