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

    Tempus ECG-Low EF

    K Number: K250119 · Decision Jul 15, 2025
    View on FDA
    Classifications
    1
    FEI Numbers
    4
    Registration Numbers
    4
    Same Product Code
    4
    Applicant Total
    3
    Review Days
    180

    Basic Information

    Device Name
    Tempus ECG-Low EF
    K Number
    K250119
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2380
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Tempus AI, Inc.
    Date Received
    January 16, 2025
    Decision Date
    July 15, 2025
    Product Code
    QYE
    Advisory Committee
    Cardiovascular
    Review Advisory Committee
    CV
    Third Party
    N

    Classifications

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

    Product Code Device Name
    QYE Reduced Ejection Fraction Machine Learning-Based Notification Software

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