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See today's BioWorld MedTech
Home » Paige receives FDA de novo authorization for AI product for prostate cancer detection
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Paige receives FDA de novo authorization for AI product for prostate cancer detection

Sep. 22, 2021
By Annette Boyle
The FDA granted de novo marketing authorization for Paige Prostate, artificial intelligence (AI)-driven software that improves detection of prostate cancer. The clinical study submitted to the FDA demonstrated that using Paige Prostate resulted in a 7% improvement in sensitivity in correctly diagnosing cancer, increasing from 89.5% to 96.8%.
BioWorld MedTech Regulatory Artificial intelligence Cancer Diagnostics Software Digital health De novo FDA

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