Saturday, March 23, 2019

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Genetesis CardioFlux™ platform receives FDA 510(k) clearance

(CincyTech) Genetesis, a medical technology company focused on using biomagnetic imaging to enable rapid, noninvasive and accurate chest pain triage, has received FDA 510(k) clearance for its cardiac imaging platform. The platform pairs the CardioFlux™ Magnetocardiograph with the integrated Faraday Analytical Cloud™ (FAC).

from EurekAlert! - Technology, Engineering and Computer Science https://ift.tt/2YjtpZc

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