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510(k) Data Aggregation
K Number
K232974Device Name
EKGenius Smart System
Manufacturer
Date Cleared
2023-11-17
(57 days)
Product Code
Regulation Number
870.2340Why 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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