FDA Clears GE Healthcare's X-ray AI Suite


The U.S. Food and Drug Administration granted 510(k) clearance to GE Healthcare's Critical Care Suite -- a collection of artificial intelligence (AI) algorithms embedded on a mobile X-ray device, the healthcare business division of GE announced today. Using GE Healthcare's Edison platform, the AI aims to help reduce the turnaround time it takes radiologists to review suspected pneumothorax, a type of collapsed lung. "By integrating AI into every aspect of care, we will ultimately improve patient outcomes, reduce waste and inefficiencies and eliminate costly errors," said Kieran Murphy, president and CEO of GE Healthcare. If a patient is scanned on a device with Critical Care Suite, it will automatically analyze the images by searching for a pneumothorax, GE Healthcare claims. If suspected, an alert with the original X-ray is sent straight to the radiologist to review.

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