FDA gives clearance to Philips for its AI powered MRI scans

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FDA gives clearance to Philips for its AI powered MRI scans
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The artificial intelligence software speeds up the process of taking scans.

, requires device manufacturers to register, and notify FDA of their intent to market a medical device at least 90 days in advance.MRCAT Head and Neck, short for MR for Calculating Attenuation, allows for the use of MRI as the main imagining modality without oncologists needing to use a CT scan. The AI software creates images that look like CT scan images, in terms of accuracy and resolution. The MRCAT takes less than three minutes to complete.

. It was said to be the industry-first online marketplace that offered curated, readily available AI resources.“The quality of your AI is only as good as the quality of the data you feed into it,” said Jeroen Tas, chief innovation & strategy officer at Philips. “We have designed HealthSuite Insights to be used by the people who work with patient data on a daily basis and have the contextual understanding, including doctors, clinicians and hospital managers.

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