Wow - they refer to the 'pulse' as if it is already FDA cleared ??? (I thought it isn't a medical device until and unless cleared) - so a lot of confidence. Does this mean it is closer to clearance than intimated during the quarterly prez ?
Use of Pulse to increase medical trials to patients who would be harder to manage over a long period and increase trail participants is a great use of the product.
News: CDX CardieX Unit Partners With Power To Increase Patient Access In Clinical Trials, page-3
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