Philips N.V. (PHG) Announces Receipt of FDA Marketing Clearance for Lumify
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Philips receives FDA 510(k) clearance for Lumify's S4-1 transducer bringing new capabilities, including cardiac imaging, to this smart-device ultrasound
October 14, 2016 10:10 AM EDTAMSTERDAM and LAS VEGAS, Oct. 14, 2016 /PRNewswire/ --Â Royal Philips (NYSE: PHG AEX: PHIA) today announced at The American College of Emergency Physicians' (ACEP) annual meeting that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market its innovative S4-1 cardiac transducer for Lumify, its smart-device diagnostic ultrasound solution. The pocket-sized and... More
