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

    SUCTION-HEMORRHOID-LIGATOR

    K Number: K832192 · Decision Dec 27, 1983
    View on FDA
    Classifications
    1
    FEI Numbers
    87
    Registration Numbers
    87
    Same Product Code
    21
    Applicant Total
    1
    Review Days
    172

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    Basic Information

    Device Name
    SUCTION-HEMORRHOID-LIGATOR
    K Number
    K832192
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.4400
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Applicant
    Research Endoscope Systems Intl.
    Date Received
    July 8, 1983
    Decision Date
    December 27, 1983
    Product Code
    FHN
    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
    FHN Ligator, Hemorrhoidal

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