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

    LIEBEL-FLARSHEIM SERIES 8000 BUCKY,W/NON SIZE SENS

    K Number: K903160 · Decision Aug 8, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    22
    Registration Numbers
    22
    Same Product Code
    26
    Applicant Total
    27
    Review Days
    21

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    Basic Information

    Device Name
    LIEBEL-FLARSHEIM SERIES 8000 BUCKY,W/NON SIZE SENS
    K Number
    K903160
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1980
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Applicant
    Continental X-Ray Corp.
    Date Received
    July 18, 1990
    Decision Date
    August 8, 1990
    Product Code
    IXQ
    Advisory Committee
    Radiology
    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
    IXQ Table, Radiographic, Stationary Top

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