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

    JEJUNOSTOMY KIT

    K Number: K831847 · Decision Aug 31, 1983
    View on FDA
    Classifications
    1
    FEI Numbers
    228
    Registration Numbers
    229
    Same Product Code
    648
    Applicant Total
    4
    Review Days
    84

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    Basic Information

    Device Name
    JEJUNOSTOMY KIT
    K Number
    K831847
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.5980
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Applicant
    Accu-Line
    Date Received
    June 8, 1983
    Decision Date
    August 31, 1983
    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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    Other Clearances by Accu-Line

    K Number Device Name
    K831636 PERCUTANEOUS INTRODUCER KIT
    K831637 ACCU-FLUSH
    K830298 ACCU-LINE SURGICAL MARKER