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

    MOVABLE CANTILEVERED RADIOGRAPHIC TABLE XRT 100, 200 & 300

    K Number: K960083 · Decision Jul 24, 1996
    View on FDA
    Classifications
    1
    FEI Numbers
    22
    Registration Numbers
    22
    Same Product Code
    26
    Applicant Total
    9
    Review Days
    195

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    Basic Information

    Device Name
    MOVABLE CANTILEVERED RADIOGRAPHIC TABLE XRT 100, 200 & 300
    K Number
    K960083
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1980
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Wuestec Medical, Inc.
    Date Received
    January 11, 1996
    Decision Date
    July 24, 1996
    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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