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FDA grants breakthrough status to Aidoc’s AI radiology report system
The FDA has granted breakthrough device designation to Aidoc’s First Read, an AI system that produces preliminary radiology report text based on chest radiograph analysis. First Read aims to address interpretation bottlenecks by producing preliminary, high-quality report drafts. The clinical AI platform is used in nearly 2,000 hospitals worldwide. Credit: Chinnapong / Shutterstock.com. The US Food and Drug Administration (FDA) has granted breakthrough device designation to Aidoc’s First Read, an AI system that produces preliminary radiology report text based on chest radiograph analysis. The company’s announcement follows an ongoing increase in imaging demand and growing concerns about interpretation delays within…
The FDA has granted breakthrough device designation to Aidoc’s First Read, an AI system that produces preliminary radiology report text based on chest radiograph analysis.
Source: Medical Device Network