Bering Secures FDA Clearance for AI-Based Chest X-Ray Triage Solution
- FDA 510(k) clearance for AI Radiology software product, targeting emergency cases found on chest X-Rays.
- Bering to accelerate business in the US market, leveraging new and existing partnerships
Bering's BraveCX is a radiological computer-assisted triage and notification software that analyzes adult (≥18 years old) chest X-ray (CXR) images for the presence of pre-specified suspected clinical findings. The product was designed to triage and prioritise emergency cases such as pleural effusion and pneumothorax immediately after the exam. Findings are notified to the physician, providing a "second opinion" and reducing the time-to-diagnosis of urgent cases.
The product was developed on over 1,000,000 CXRs acquired across diverse clinical settings and further fine-tuned with over 50,000 CXRs labelled by board-certified radiologists. BraveCX shows excellent performance of 95%-97% specificity and ROC AUCs of 0.96 and 0.98 on pleural effusion and pneumothorax respectively.
The FDA clearance allows the company to accelerate its sales expansion in the US market. Using a flexible deployment model of a cloud-based service, directly on premises, or integrated with CXR hardware systems, Bering can leverage new and existing partnerships to rapidly bring this device to market.
Dr.
About
Bering Limited is a medical AI software company that creates Clinical Decision Support systems along the continuum of health and care. Founded in 2010, Bering is internationally acknowledged for its state-of-the-art research and its application to translational medicine. Bering is based in
View original content:https://www.prnewswire.com/news-releases/bering-secures-fda-clearance-for-ai-based-chest-x-ray-triage-solution-302007589.html
SOURCE Bering Research
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