PHG News & Events

Philips announced it has received FDA 510(k) clearance for EchoNavigator R5.0 with DeviceGuide, an AI-powered software solution that assists physicians during one of interventional cardiology's most technically demanding procedures - repairing leaking mitral valves through a minimally invasive approach.

Philips has announced the launch of its interventional guidance platform, IntraSight Plus, which is cleared for clinical use in the USA and Europe. With CE marking and FDA 510 clearance, the redesigned platform combines diagnostic and treatment planning tools. By streamlining access to interventional tools, IntraSight Plus enables clinicians to diagnosis, virtually plan treatment, guide device placement and verify results all on a single screen.