GE HealthCare has announced the Food and Drug Administration (FDA) 510 (k) clearance for its SIGNA MAGNUS magnetic resonance ...
CHICAGO--GE HealthCare (Nasdaq: GEHC) has received FDA 510(k) clearance for its innovative SIGNAâ„¢ MAGNUS,i a 3.0T ...
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 ...
GE HealthCare on Wednesday said U.S. regulators had cleared its head-only magnetic resonance imaging scanner.
GE HealthCare Technologies Inc. GEHC is scheduled ... In May, GEHC launched a head-only MR scanner, SIGNA MAGNUS, to address the limitations of whole-body MR scanners. The Revolution RT was ...
GE HealthCare Technologies Inc. GEHC is scheduled to report third-quarter 2024 results on Oct. 30, before market open. In the ...
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, ...