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

    SONOSITE MAXX SERIES ULTRASOUND SYSTEM

    K Number: K130173 · Decision Mar 25, 2013
    View on FDA
    Classifications
    1
    FEI Numbers
    211
    Registration Numbers
    211
    Same Product Code
    1117
    Applicant Total
    7
    Review Days
    60

    Basic Information

    Device Name
    SONOSITE MAXX SERIES ULTRASOUND SYSTEM
    K Number
    K130173
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1550
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    FUJIFILM SONOSITE,INC.
    Date Received
    January 24, 2013
    Decision Date
    March 25, 2013
    Product Code
    IYN
    Advisory Committee
    Radiology
    Review Advisory Committee
    RA
    Third Party
    Y

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    IYN System, Imaging, Pulsed Doppler, Ultrasonic

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