(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 ...
PK Study Successfully Demonstrates that Fingerprint Sweat Provides Reliable Sample for Drug DetectionFDA 510(k) Clearance ...
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 YORK, Nov. 13, 2024 /PRNewswire/ -- Fourth Frontier, a medical technology company based out of New York and Bangalore, announced the 510(k) clearance of the Frontier X Plus from the U.S. FDA. The ...
The products are part of the agency's ongoing public health alert concerning cinnamon with elevated lead levels ...
Cad (Nasdaq:ICAD) announced today that the FDA cleared its ProFound Detection version 4.0 for digital breast tomosynthesis ...
Philips announced that the FDA granted 510(k) clearance for its new detector-based spectral computed tomography (CT) ...
Hyperfine, Inc. (Nasdaq: HYPR), the groundbreaking health technology company that has redefined brain imaging with the first ...
Hyperfine, Inc. announced the presentation of additional research data and images using the Swoop® system to image patients ...
WASHINGTON, D.C.—Johnson & Johnson MedTech’s Abiomed announced that its compressible, expandable heart pump has cleared a pivotal trial, and it’s now headed for FDA review in the coming months.
So why wouldn’t you want to get it under control if at all possible? You can and should, thanks to ZQuiet, an FDA-cleared snoring solution that you can save big on right now. With this special offer, ...
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