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Genetesis Receives 2nd FDA Breakthrough Device Designation for Non-Invasive Diagnosis of Myocardial Ischemia Using CardioFlux MCG
Designation represents progress for patients with suspected Coronary Microvascular Dysfunction as the FDA recognizes disease’s debilitating impacts and the lack of effective non-invasive options for efficient diagnosis
United states
Robert takla
Timothy henry
Odayme quesada
Drug administration
Christ hospital lindner center
Christ hospital health network
European society of cardiology
Women heart center
Genetesis inc
Breakthrough device
Christ hospital
Medical director
Heart center
Principal investigator
European society
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