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Imbio Receives FDA 510(k) Clearance for New Cardiothoracic Imaging Algorithm
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MINNEAPOLIS, March 16, 2021 /PRNewswire/ Imbio, a leading provider of artificial intelligence (AI) solutions for medical imaging analysis, has received U.S. Food and Drug Administration (FDA) 510(k) clearance for its RV/LV Analysis™ algorithm.
The RV/LV Analysis algorithm is a rapid, automated assessment of potential right ventricular dilation. The tool quickly and accurately measures the ventricles of the heart to provide the ratio of the maximum diameter of the right versus the left ventricle. The resulting RV/LV ratio is a key patient risk indicator for various pulmonary conditions such as pulmonary embolism (PE). RV/LV Analysis results are automatically available for clinicians without any additional work including a full report of quantitative findings added directly to the patient imaging study within minutes.