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

    UR 150-UR 150T

    K Number: K801723 · Decision Aug 13, 1980
    View on FDA
    Classifications
    1
    FEI Numbers
    5
    Registration Numbers
    5
    Same Product Code
    7
    Applicant Total
    66
    Review Days
    20

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    Basic Information

    Device Name
    UR 150-UR 150T
    K Number
    K801723
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    876.4890
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Applicant
    Siemens Corp.
    Date Received
    July 24, 1980
    Decision Date
    August 13, 1980
    Product Code
    KQS
    Advisory Committee
    Gastroenterology, Urology
    Review Advisory Committee
    RA
    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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