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Aidoc 510(k) for Pulmonary Embolism AI Cleared
05/15/2019
 

FDA has cleared an Aidoc 510(k) for its pulmonary embolism (PE) artificial intelligence (AI) product that helps radiologists flag and triage PE cases in chest computerized tomography scans. The company’s AI analyzes medical images directly after the patient is scanned and notifies radiologists on cases with suspected findings to assist with prioritization of time-sensitive, and potentially life-threatening cases. The AI “cuts the time from scan to diagnosis for some patients from hours to under five minutes, speeding up treatment and improving prognosis,” the company says.


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