RapidAI earns FDA clearance for PE triage software

AuntMinnie.com staff writers
May 23, 2022
2018 08 01 23 13 1733 Artificial Intelligence Ai 400

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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