GE HealthCare wins FDA clearance for Allia Moveo interventional imaging system
6 Articles
6 Articles
GE HealthCare’s Allia Moveo gains FDA and CE mark approvals
GE HealthCare’s Allia Moveo system GE HealthCare has announced that its Allia Moveo image-guidance platform has received US Food and Drug Administration (FDA) 510(k) clearance and CE mark. The latest Allia platform was first unveiled at the Radiological Society of North America’s (RSNA) 2025 annual meeting (30 November–4 December, Chicago, USA). GE says that the new system will assist clinicians in a wide range of cardiovascular, vascular, non-v…
GE HealthCare gains US-EU approval for Allia Moveo imaging system
GE HealthCare has gained simultaneous US Food and Drug Administration (FDA) clearance and a European CE mark for Allia Moveo, setting healthcare centres up with an imaging system intended to facilitate greater procedural flexibility in the interventional suite.The post GE HealthCare gains US-EU approval for Allia Moveo imaging system appeared first on Medical Device Network.
GE HealthCare Receives FDA Clearance for Allia Moveo Interventional Imaging System
Allia Moveo What You Should Know The Launch: GE HealthCare has received FDA 510(k) clearance and CE Marking for Allia Moveo, a new mobile C-arm system designed for cardiovascular and interventional procedures.The Design: The system addresses the physical constraints of the operating room. It is compact and cable-free, featuring a “wide-bore” design that accommodates patients of any size while allowing effortless table panning.The AI: The platfor…
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