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

    LEONARD TUBE

    K Number: K892334 · Decision May 31, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    12
    Registration Numbers
    12
    Same Product Code
    22
    Applicant Total
    6
    Review Days
    56

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    Basic Information

    Device Name
    LEONARD TUBE
    K Number
    K892334
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.5980
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Applicant
    Surgidyne, Inc.
    Date Received
    April 5, 1989
    Decision Date
    May 31, 1989
    Product Code
    KDH
    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
    KDH Catheter (Gastric, Colonic, Etc.), Irrigation And Aspiration

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    K852180 SURGIDYNES VARIDYNE 350-2I & 350-2C CORDLESS ELEC.
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