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FDA Grants 510(k) Clearance To Viz.ai’s Viz Subdural Plus Module - Data Intelligence

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Viz.ai leverages AI algorithms and machine learning to expedite diagnosis and care. Credit: T Schneider / Shutterstock. The US Food and Drug Administration (FDA) has granted 510(k) clearance to Viz.ai for its Viz Subdural Plus module, designed for enhancing clinical decision-making. It is claimed to be the first solution to quantify the size of collections such as subdural haemorrhages (SDH) in the subdural space on non-contrast computed tomogra…
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Medical Device Network broke the news in on Friday, June 13, 2025.
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