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RapidAI Secures FDA Clearance for Five New Deep Clinical AI Modules, Expanding Enterprise Imaging Platform

RapidAI Secures FDA Clearance for Five New Deep Clinical AI Modules, Expanding Enterprise Imaging Platform

What You Should Know: 

– RapidAI, a pioneer in deep clinical AI, announced U.S. FDA clearance for five new imaging modules—Rapid DeltaFuse, Rapid LMVO, Rapid MLS, Rapid OH, and Rapid Aortic for measurement. 

– The expansion reinforces the Rapid Enterprise Platform’s focus on bringing deep clinical intelligence and seamless workflow integration across the entire patient journey.

Deep Clinical AI: Shifting Beyond Triage to Full Patient Management

RapidAI’s latest FDA clearances underscore its commitment to building deep clinical AI—algorithms that move beyond simple triage to support superior decision-making in both acute and long-term settings.

The five new modules focus on providing precision, quantification, and automation across neurology and vascular care:

The new capabilities directly address cognitive burden for radiologists. By pairing imaging precision with automation, the modules reduce interpretation time and eliminate manual measurement variability.

Source: hitconsultant.net –

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