GE HealthCare (Nasdaq:GEHC) announced today that it received FDA 510(k) clearance for its Signa Magnus MRI scanner.

GE HealthCare on Wednesday said U.S. regulators had cleared its head-only magnetic resonance imaging scanner. The Chicago-based medical technology company said the MRI device, called Signa Magnus, had ...

New atomic sensor technology enhances MRI quality control by tracking hyperpolarized molecules in real-time, with potential ...

(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 ...

Discover how Remedy Logic's FDA-cleared RAI program, powered by AI, is revolutionizing spine MRI interpretation for radiologists and patients.

Workflow Improvement Across All Scanners: Vendor-neutral software that improves image quality for both regular and accelerated protocols. Increased Efficiency and Capacity: Higher scan capacity and ...