BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    STOMAHESIVE POWDER

    K Number: K792382 · Decision Dec 20, 1979
    View on FDA
    Classifications
    1
    FEI Numbers
    90
    Registration Numbers
    90
    Same Product Code
    100
    Applicant Total
    32
    Review Days
    24

    Basic Information

    Device Name
    STOMAHESIVE POWDER
    K Number
    K792382
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    876.5900
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Applicant
    E. R. SQUIBB & SONS, INC.
    Date Received
    November 26, 1979
    Decision Date
    December 20, 1979
    Product Code
    EXB
    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
    EXB Collector, Ostomy

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