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

    VIABIL BILIARY ENDOPROSTHESIS

    K Number: K041423 · Decision Jul 21, 2004
    View on FDA
    Classifications
    1
    FEI Numbers
    143
    Registration Numbers
    143
    Same Product Code
    473
    Applicant Total
    163
    Review Days
    54

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    Basic Information

    Device Name
    VIABIL BILIARY ENDOPROSTHESIS
    K Number
    K041423
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    876.5010
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Unknown
    Statement or Summary
    Summary
    Applicant
    W. L. Gore & Associates, Inc.
    Date Received
    May 28, 2004
    Decision Date
    July 21, 2004
    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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