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    FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

    EPX-Series Mobile X-ray System

    K Number: K151038 · Decision Jul 24, 2015
    View on FDA
    Classifications
    1
    FEI Numbers
    77
    Registration Numbers
    77
    Same Product Code
    235
    Applicant Total
    4
    Review Days
    95

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    Basic Information

    Device Name
    EPX-Series Mobile X-ray System
    K Number
    K151038
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1720
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Ecotron Co., Ltd.
    Date Received
    April 20, 2015
    Decision Date
    July 24, 2015
    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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    Other Clearances by Ecotron Co., Ltd.

    K Number Device Name
    K221233 DT-703
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