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 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 ...
GE HealthCare Technologies Inc. GEHC is scheduled to report third-quarter 2024 results on Oct. 30, before market open. In the last reported quarter, the company’s adjusted earnings per share of ...
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Lower Volume Likely to Hurt GE HealthCare's Q3 EarningsGE 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, ...
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