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 ...

CHICAGO--GE HealthCare (Nasdaq: GEHC) has received FDA 510(k) clearance for its innovative SIGNA™ 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 ...

The system is designed to shorten scan times, which may be better for people who struggle to stay still or have claustrophobia, and to detect more subtle abnormalities.

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 ...

Analyst Larry Biegelsen of Wells Fargo maintained a Buy rating on GE Healthcare Technologies Inc (GEHC – Research Report), retaining the ...

GE HealthCare announced that its Brazil-based partner Ionic Health received FDA 510(k) clearance for its nCommand Lite, which provides diagnostic imaging centers with real-time scanning, remote ...