FDA clears Philips AI solution that provides real-time guidance during complex minimally invasive heart valve repair
Royal Philips has received FDA 510(k) clearance for DeviceGuide, an AI-powered software integrated with EchoNavigator R5.0 and the Azurion platform, designed to provide real-time guidance during complex minimally invasive mitral valve repairs. Developed in collaboration with Edwards Lifesciences, DeviceGuide assists physicians by fusing live echoca…