BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇯🇵 Japan

    UltraExtend NX CUW-U001S V2.0 Ultrasound Image Analysis Program

    K Number: K250328 · Decision Apr 30, 2025
    View on FDA
    Classifications
    1
    FEI Numbers
    217
    Registration Numbers
    217
    Same Product Code
    303
    Applicant Total
    97
    Review Days
    84

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    Basic Information

    Device Name
    UltraExtend NX CUW-U001S V2.0 Ultrasound Image Analysis Program
    K Number
    K250328
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.2050
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Canon Medical Systems Corporation
    Date Received
    February 5, 2025
    Decision Date
    April 30, 2025
    Product Code
    QIH
    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
    QIH Automated Radiological Image Processing Software

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