BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

    EndoGI Biliary Stent System

    K Number: K193600 · Decision Jun 26, 2020
    View on FDA
    Classifications
    1
    FEI Numbers
    143
    Registration Numbers
    143
    Same Product Code
    473
    Applicant Total
    2
    Review Days
    186

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    Basic Information

    Device Name
    EndoGI Biliary Stent System
    K Number
    K193600
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.5010
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Endogi Medical, Ltd.
    Date Received
    December 23, 2019
    Decision Date
    June 26, 2020
    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 Endogi Medical, Ltd.

    K Number Device Name
    K232596 EndoGI S-Path Biliary Stent System