www.fdanews.com/articles/188935-fda-oks-philips-intellivue-mobile-app
FDA OK’s Philips’ IntelliVue Mobile App
October 25, 2018
The FDA granted 510(k) clearance for Philips’ Intellivue GuardianSoftware mobile application, which allows clinicians to see a patients’ vital signs and early warning signs through a mobile device.
The app provides clinicians with real-time data so that they can receive warning of patient deterioration before adverse events occur.
The mobile app is designed to be compatible with certain wearable devices, such as biosensors.