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

    HYDRADJUST II UROLOGICAL TABLE

    K Number: K791699 · Decision Oct 22, 1979
    View on FDA
    Classifications
    1
    FEI Numbers
    5
    Registration Numbers
    5
    Same Product Code
    7
    Applicant Total
    37
    Review Days
    54

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    Basic Information

    Device Name
    HYDRADJUST II UROLOGICAL TABLE
    K Number
    K791699
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    876.4890
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Applicant
    Sybron Corp.
    Date Received
    August 29, 1979
    Decision Date
    October 22, 1979
    Product Code
    KQS
    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
    KQS Table, Cystometric, Non-Electric And Accessories

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