RapidAI earns FDA clearance for PE triage software

By AuntMinnie.com staff writers

May 24, 2022 -- Artificial intelligence (AI) software developer RapidAI has secured U.S. Food and Drug Administration (FDA) 510(k) clearance for its Rapid PE Triage & Notification software platform.

Rapid PE Triage & Notification is designed to identify suspected cases of central pulmonary embolism (PE) on CT pulmonary angiography exams and provide real-time notifications to physicians, according to the vendor.


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