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FDA clears Epredia’s digital pathology solution
Epredia has received 510(k) clearance from the US Food and Drug Administration ... E1000 Dx comprises an automated digital ...
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FDA grants 510(k) clearance to GE HealthCare’s updated ultrasound systems
The US Food and Drug Administration (FDA) has granted 510(k) clearance to GE HealthCare ... healthcare by integrating ‘high-resolution’ image quality with the latest ultrasound technology ...
Business Wire15d
Epredia Receives U.S. FDA 510(K) Clearance for the E1000 Dx™ Digital Pathology Solution Designed to Improve Laboratory Workflow in Cancer Diagnostics
--(BUSINESS WIRE)--Epredia, a global leader in precision cancer diagnostics and subsidiary of PHC Holdings Corporation (TSE: 6523), today announced U.S. Food and Drug Administration (FDA) 510 ...