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

    HOLLISTER VERTICAL DRAIN/TUBE ATTACHMENT DEVICE

    K Number: K932855 · Decision Oct 13, 1993
    View on FDA
    Classifications
    1
    FEI Numbers
    242
    Registration Numbers
    243
    Same Product Code
    648
    Applicant Total
    85
    Review Days
    125

    Basic Information

    Device Name
    HOLLISTER VERTICAL DRAIN/TUBE ATTACHMENT DEVICE
    K Number
    K932855
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.5980
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    HOLLISTER, INC.
    Date Received
    June 10, 1993
    Decision Date
    October 13, 1993
    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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