Philips scores FDA nod for DR system

By staff writers

February 20, 2019 -- Philips Healthcare has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market its DigitalDiagnost C90 premium digital radiography (DR) system.

DigitalDiagnost C90 features the Philips Eleva common user interface, which extends to the Eleva tube head to speed workflow and offers a touchscreen display to transfer operation into the exam room for more time with the patient.

Unique 2 image processing and bone suppression software are also available to help radiologists process clearer images for better diagnoses and to reduce the chances of a rescan.

Copyright © 2019

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