Tempus AI Receives the US FDA’s 510(k) Clearance for Updated Tempus Pixel Cardiac Imaging Platform


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  • Tempus AI has received the US FDA 510(k) clearance for its updated Tempus Pixel, an AI-powered cardiac imaging platform, with the ability to generate T1 & T2 inline maps for enhanced cardiac MRI analysis
  • Tempus Pixel delivers advanced viewing & automated reporting of cardiac MR images, improving efficiency and accuracy in flow visualization, functional analysis, & tissue characterization to support faster, more informed clinical decisions
  • The newly cleared functionality enables direct creation of T1 & T2 maps from raw MRI data, providing precise tissue characterization & generating detailed DICOM maps to detect fibrosis, inflammation, or edema

Ref: Tempus | Image: Tempus Press Release

Related News:- Imagene Partners with Tempus AI to Develop AI-Powered Diagnostics for NSCLC

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