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

    MODIF TOP DRIVE BOARD CXT-90 90/90 DIAG TILT TABLE

    K Number: K912996 · Decision Feb 3, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    23
    Registration Numbers
    23
    Same Product Code
    76
    Applicant Total
    27
    Review Days
    210

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    Basic Information

    Device Name
    MODIF TOP DRIVE BOARD CXT-90 90/90 DIAG TILT TABLE
    K Number
    K912996
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1980
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Continental X-Ray Corp.
    Date Received
    July 8, 1991
    Decision Date
    February 3, 1992
    Product Code
    IXR
    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
    IXR Table, Radiographic, Tilting

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