BRIEF-Philips Receives U.S. FDA 510(K) Clearance To Market Proxidiagnost N90
March 15, 2018 at 10:25 AM EDT
* PHILIPS RECEIVES U.S. FDA 510(K) CLEARANCE TO MARKET PROXIDIAGNOST N90, ITS PREMIUM DIGITAL RADIOGRAPHY AND NEARBY FLUOROSCOPY SYSTEM Source text for Eikon: Further company coverage: (Gdynia Newsroom)
