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

    THE KEOFEED STOMACH TUBE

    K Number: K812507 · Decision Sep 14, 1981
    View on FDA
    Classifications
    1
    FEI Numbers
    228
    Registration Numbers
    229
    Same Product Code
    648
    Applicant Total
    4
    Review Days
    13

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    Basic Information

    Device Name
    THE KEOFEED STOMACH TUBE
    K Number
    K812507
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.5980
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Applicant
    Hedeco
    Date Received
    September 1, 1981
    Decision Date
    September 14, 1981
    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 Hedeco

    K Number Device Name
    K830497 PEM-T
    K822380 ROMBEAU GASTROSTOMY-JEJUNAL TUBE
    K820063 KEOFEED 500 ENTERIC FEEDING PUMP