FDA allows marketing of non-invasive device to help evaluate heart blood flow

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Title: FDA allows marketing of non-invasive device to help evaluate heart blood flow

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11/26/2014 11:45 AM EST

The U.S. Food and Drug Administration today allowed marketing of the HeartFlow FFR-CT software, which permits health care professionals to non-invasively evaluate blood flow in the coronary arteries of patients showing signs and symptoms of coronary artery disease.

 

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