Philips Gains FDA’s 510(k) Clearance for Its MR 7700 Diagnostic System

Royal Philips has received the FDA’s 510(k) marketing clearance for its MR 7700 3.0T magnetic resonance system.

The system, which features integrated multinuclei imaging and spectroscopy, adds metabolic information to magnetic resonance images to help improve clinical decisionmaking.

The system allows radiologists to image six clinically relevant nuclei in different body types. It features artificial intelligence software that enables connected imaging, optimized workflows and clinical solutions, the company said.