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 ...
The system is designed to shorten scan times, which may be better for people who struggle to stay still or have ...
GE HealthCare says the head-only design allows the system to deliver a gradient amplitude and slew rate far surpassing those ...
CHICAGO--GE HealthCare (Nasdaq: GEHC) has received FDA 510(k) clearance for its innovative SIGNAâ„¢ MAGNUS,i a 3.0T ...
(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 ...
GE HealthCare on Wednesday said U.S. regulators had cleared its head-only magnetic resonance imaging scanner.
New MRI technology aims to advance neuroimaging and biomarker research CHICAGO--(BUSINESS WIRE)-- GE HealthCare (Nasdaq: GEHC) has received FDA 510(k) clearance for its innovative SIGNAâ„¢ MAGNUS ...
GE HealthCare (Nasdaq: GEHC) has received FDA 510(k) clearance for its innovative SIGNAâ„¢ MAGNUS,i a 3.0T high-performance, head-only magnetic resonance imaging (MRI) scanner. This system offers new ...