Paige Receives the US FDA's 510(k) Clearance for its FullFocus Viewer to Use in Digital Pathology
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- The FullFocus viewer allows pathologists to view and navigate images when used together with the Philips’ Ultra-Fast scanner. The AI firm is working to expand the 510(k) clearance to include the use of FullFocus with additional scanners and monitors in future
- In Nov’2019- FullFocus received the CE Mark- making it available to use in the EU. Paige has early access trials across the US- EU- and Brazil with healthcare organizations to serve patients and maintains a business continuity
- FullFocus operates within the Paige Platform and allows users- meaning researchers and pathologists to view any digital image- regardless of the scanning platform used to generate the image
Ref: Businesswire | Image: Paige
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