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510(k) Data Aggregation

    K Number
    K232974
    Device Name
    EKGenius Smart System
    Manufacturer
    Date Cleared
    2023-11-17

    (57 days)

    Product Code
    Regulation Number
    870.2340
    Why did this record match?
    Applicant Name (Manufacturer) :

    EKGenius LLC

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    The EKGenius Smart System is intended to acquire a resting, diagnostic 12-lead ECG for display and subsequent upload to EKGenius Smart System software, which is installed on an iPad or iPhone. This enables clinicians, or trained care personnel who are acting on the orders of a licensed physician, to acquire, store, and print diagnostic 12lead ECGs. The EKGenius Smart System is for use on adult and pediations, diseased or non-diseased and is not intended for use on neonatal (birth to 28 days) or infants (29 days up to 2 years). The device is not for use as a vital signs physiological monitor. The EKGenius Smart System is intended to be used for clinical use rather than home used in a professional healthcare facility, or a clinical environment such as clinics. It cannot be used in transport environment, such as ambulance. The EKGenius Smart System provides uninterpreted 12-lead ECG data and is not to be a sole means of diagnosis.
    Device Description
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