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

    AVD INTIMAX (TM) BILIARY CATHETER

    K Number: K910006 · Decision Feb 13, 1991
    View on FDA
    Classifications
    1
    FEI Numbers
    143
    Registration Numbers
    143
    Same Product Code
    473
    Applicant Total
    2
    Review Days
    42

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    Basic Information

    Device Name
    AVD INTIMAX (TM) BILIARY CATHETER
    K Number
    K910006
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.5010
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Applicant
    Applied Vascular
    Date Received
    January 2, 1991
    Decision Date
    February 13, 1991
    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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    Other Clearances by Applied Vascular

    K Number Device Name
    K923699 DIAGNOSTIC INTRAVASCULAR CATHETER