Philips

Philips announced that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its Ingenia Elition 3.0T magnetic resonance imaging (MRI) solution and two clinical applications, Philips Compressed Sense and 3D APT. This integrated suite of innovations enables clinicians to perform exams up to 50 percent faster [1], increase diagnostic confidence and improve the patient experience.

Many say it is very difficult or impossible to go through the large volumes of data to pick out what is clinically ...

Philips Healthcare last week issued a proactive advisory warning to its iSite and IntelliSpace picture archiving and communication system (PACS) customers of potential security vulnerabilities in the products. The company cautioned that while it has received no reports of patient harm, the vulnerabilities in question could impact or potentially compromise patient confidentiality, system integrity and/or system availability.

Philips in partnership with Innovative Imaging Technologies (IIT) announced an industry-first integrated tele-ultrasound solution on Philips’ Lumify portable ultrasound system powered by IIT’s Reacts collaborative platform. This innovation connects clinicians around the globe in real time by turning a compatible smart device into an integrated tele-ultrasound solution, combining two-way audio-visual calls with live ultrasound streaming.

March 15, 2018 – Philips announced it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to ...