FDA 510(k) Clearance Granted to Philips Rembra Platform

Philips has secured FDA 510(k) clearance for its Rembra platform of scanning systems, marking a regulatory milestone for its latest computed tomography technologies. The clearance covers the Rembra CT, Rembra RT and Areta RT systems, which are positioned to support both diagnostic imaging and radiation therapy planning. The company had introduced the Rembra CT system […]

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