GE HealthCare secures FDA 510(k) clearance for diagnostic viewer

View offers 2D and 3D visualisation, along with AI-based tools, to assist in clinical decision making.

GE HealthCare has received 510(k) clearance from the US Food and Drug Administration (FDA) for View, the diagnostic viewer within its Genesis Radiology Workspace.

The new solution is designed as a fast, zero-footprint diagnostic viewer and aims to streamline workflows and increase precision in radiological practice.

Evidence indicates radiologists spend up to 44% of their time on tasks unrelated to image interpretation such as interface navigation or waiting for images to load.

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