GE HealthCare  has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for True Definition DL,ii  the latest addition…
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Cara Medical Ltd. recently announced that the U.S. Food and Drug Administration (FDA) has granted 510(k) clearance for the CARA System, a computed tomography angiography (CTA)-based platform that provides noninvasive, patient-specific three-dimensional (3D) visualization of the cardiac conduction system.
The MEDRAD Centargo CT Injection System helps reduce process and administrative burdens for healthcare providers, enabling them to focus more on patient care, particularly in high throughput settings.
Built on GE HealthCare’s proprietary Deep Silicon detector technology, Photonova Spectra is designed to deliver remarkable spectral and spatial resolution for ultra-high-definition (UHD) imaging with wide coverage.
Arineta, a leader in advancing cardiovascular imaging solutions, recently announced that Yuma Cardiac Center and Yuma Cardiology Associates have partnered to bring the SpotLight cardiac CT scanner to Southwest Arizona for the first time, according to a news release.
At the annual Transcatheter Cardiovascular Therapeutics (TCT 2025) meeting, Royal Philips introduced an industry-first innovation that integrates pre-operative CT data directly into the cath lab workflow, according to a press release.
The United States Food and Drug Administration (FDA) issued a 510(k) clearance letter for the Planmed XFI full-body CT scanner on September 26, 2025.
University Hospitals health system in Cleveland recently became the first healthcare institution in the United States to install the Naeotom…
GE HealthCare has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its Revolution Vibe CT system,…
CHICAGO | Building on a collaboration that spans more than three decades, GE HealthCare has renewed its research collaboration with…
