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

    SCUBA BILIARY STENT SYSTEM

    K Number: K092352 · Decision Mar 16, 2010
    View on FDA
    Classifications
    1
    FEI Numbers
    143
    Registration Numbers
    143
    Same Product Code
    473
    Applicant Total
    4
    Review Days
    224

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    Basic Information

    Device Name
    SCUBA BILIARY STENT SYSTEM
    K Number
    K092352
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.5010
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Unknown
    Statement or Summary
    Summary
    Applicant
    Invatec S.P.A.
    Date Received
    August 4, 2009
    Decision Date
    March 16, 2010
    Product Code
    FGE
    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
    FGE Stents, Drains And Dilators For The Biliary Ducts

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