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FDA clears Philips DigitalDiagnost C90 radiography system
Healthcare IT News: Health technology giant Royal Philips announced it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market its DigitalDiagnost C90 radiography system.
The ceiling-mounted radiography system features a live camera image directly displayed at the tube head, designed to increase patient throughput and decrease the time to diagnosis, Philips said.
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