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

    ViSiGi LUX (5332); ViSiGi LUX (5336); ViSiGi LUX (5340)

    K Number: K234033 · Decision May 6, 2024
    View on FDA
    Classifications
    1
    FEI Numbers
    228
    Registration Numbers
    229
    Same Product Code
    648
    Applicant Total
    5
    Review Days
    138

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    Basic Information

    Device Name
    ViSiGi LUX (5332); ViSiGi LUX (5336); ViSiGi LUX (5340)
    K Number
    K234033
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.5980
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Boehringer Laboratories, LLC
    Date Received
    December 20, 2023
    Decision Date
    May 6, 2024
    Product Code
    KNT
    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
    KNT Tubes, Gastrointestinal (And Accessories)

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