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

    AJEX 1200 H / AJEX 240H MOBILE X-RAY GENERATOR

    K Number: K122298 · Decision Mar 28, 2014
    View on FDA
    Classifications
    1
    FEI Numbers
    77
    Registration Numbers
    77
    Same Product Code
    235
    Applicant Total
    1
    Review Days
    605

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    Basic Information

    Device Name
    AJEX 1200 H / AJEX 240H MOBILE X-RAY GENERATOR
    K Number
    K122298
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1720
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Ajex Meditech., Ltd.
    Date Received
    July 31, 2012
    Decision Date
    March 28, 2014
    Product Code
    IZL
    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
    IZL System, X-Ray, Mobile

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