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

    omni TRAX Active Patient Tracker

    K Number: K143396 · Decision Jan 23, 2015
    View on FDA
    Classifications
    1
    FEI Numbers
    348
    Registration Numbers
    349
    Same Product Code
    892
    Applicant Total
    1
    Review Days
    58

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    Basic Information

    Device Name
    omni TRAX Active Patient Tracker
    K Number
    K143396
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1560
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Civco Medical Instruments CO Inc Dba Civco Medical Solutions
    Date Received
    November 26, 2014
    Decision Date
    January 23, 2015
    Product Code
    IYO
    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
    IYO System, Imaging, Pulsed Echo, Ultrasonic

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