GE HealthCare has announced the Food and Drug Administration (FDA) 510 (k) clearance for its SIGNA MAGNUS magnetic resonance ...

GE HealthCare Technologies GEHC recently announced the receipt of FDA clearance for its SIGNA MAGNUS, a 3.0T high-performance ...

GE HealthCare says the head-only design allows the system to deliver a gradient amplitude and slew rate far surpassing those ...

(RTTNews) - GE HealthCare Technologies Inc. (GEHC) Wednesday said that it has received FDA 510(k) clearance for its innovative SIGNA MAGNUS 3.0T high-performance, head-only magnetic resonance imaging ...

The National Comprehensive Cancer Network® (NCCN®)?an alliance of leading cancer centers?today announced the publication of a ...

at 08:05 GE HealthCare Receives FDA Clearance for Head-Only SIGNA MAGNUS 3.0T MRI System GE HealthCare has received FDA 510(k) clearance for its innovative SIGNAtm MAGNUS,i a 3.0T high-performance, ...

The Chicago-based medical technology company said the MRI device, called Signa Magnus, had received 510(k) clearance by the U.S. Food and Drug Administration. That approval pathway is for devices that ...

A team of AI researchers and mathematicians affiliated with several institutions in the U.S. and the U.K. has developed a math benchmark that allows scientists to test the ability of AI systems to ...

Austria’s top court ruled that a restructuring plan put forward by Signa Prime Selection AG and its creditors was unlawful, pushing the luxury landlord into bankruptcy. The Supreme Court verdict ...

Austrian court upholds verdict that restructuring not viable Rene Benko’s luxury unit now faces liquidation of its assets Austria ’s top court ruled that a restructuring plan put forward by Signa ...

(Bloomberg) -- Austria’s top court ruled that a restructuring plan put forward by Signa Prime Selection AG and its creditors was unlawful, pushing the luxury landlord into bankruptcy. The Supreme ...