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

    MWX-7440 HIGH SPEED BUCKY

    K Number: K924423 · Decision Jan 15, 1993
    View on FDA
    Classifications
    1
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    25
    Applicant Total
    3
    Review Days
    136

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    Basic Information

    Device Name
    MWX-7440 HIGH SPEED BUCKY
    K Number
    K924423
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1860
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Midwest X-Ray Equipment Co.
    Date Received
    September 1, 1992
    Decision Date
    January 15, 1993
    Product Code
    KPX
    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
    KPX Changer, Radiographic Film/Cassette

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    Other Clearances by Midwest X-Ray Equipment Co.

    K Number Device Name
    K827609 MIDWEST AUTOMATIC BUCKY EQUIPPED WITH GRID AND SIZE-O-MATIC TRAY
    K827504 SIZE SENSING CASSETTE TRAY