GE HealthCare Launches Upgrade Options for Interventional Systems
New pathways allow health systems to update legacy imaging equipment with artificial intelligence and workflow tools while preserving existing infrastructure.
New pathways allow health systems to update legacy imaging equipment with artificial intelligence and workflow tools while preserving existing infrastructure.
AI tools are enhancing medical imaging by identifying subtle patterns and anomalies, giving staff an extra layer of support without taking over the diagnostic process.
Siemens Healthineers has received U.S. FDA clearance for the AI-powered Acuson Origin cardiovascular ultrasound system and the AcuNav Lumos 4D ICE catheter, both designed to improve cardiac diagnostics and patient care.
New pathways allow health systems to update legacy imaging equipment with artificial intelligence and workflow tools while preserving existing infrastructure.
GE HealthCare announced FDA 510(k) clearance of Allia IGS Pulse – the latest addition to the company’s image guided system (IGS) offerings.
Read MoreThe FDA cleared the CorVista System with CAD Add-On to evaluate the presence of significant coronary artery disease as an aid in diagnosis.
Read MoreGetinge recalled the Cardiosave Hybrid and Rescue IABPs because they may shut down unexpectedly due to electrical failure.
Read MoreAcorai, a startup medical device manufacturer, announced that the FDA has granted Breakthrough Device Designation for Acorai’s Heart Monitor.
Read MoreGenesis MedTech announced that its J-Valve Transfemoral (TF) System has been granted Breakthrough Device designation by the FDA.
Read MoreMagAssist introduced its ECMO system BreathMo, which uses maglev technology to reduce the risk of blood damage.
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Cardiawave SA, a deeptech medical device manufacturer that developed Valvosoft, a non-invasive medical device to treat aortic stenosis, announced the issuance of three new patents in the United States.