-

RapidAI Receives FDA Clearance of Rapid LVO For Identification of Suspected Large Vessel Occlusions

MENLO PARK, Calif.--(BUSINESS WIRE)--RapidAI, the worldwide leader in advanced imaging for stroke, today announced that Rapid LVO has received Food and Drug Administration (FDA) clearance for detecting suspected LVOs (Large Vessel Occlusions).

Rapid LVO helps physicians speed up triage or transfer decision-making. Working in as few as 3 minutes, Rapid LVO uses a vessel tracker in conjunction with assessment of brain regions with reduced blood vessel density to identify suspected LVOs with a sensitivity of 97% and a specificity of 96%. Stroke team members are also immediately notified when a suspected LVO is detected.

“LVOs are the most disabling and deadly ischemic strokes,” said Dr. Greg Albers, Professor of Neurology at Stanford University, Director of the Stanford Stroke Center and cofounder of RapidAI. “The ability to identify LVOs rapidly facilitates more effective treatment. This is why we are very excited about the FDA clearance of Rapid LVO, a significant step forward in stroke diagnostics and care.”

RapidAI makes the most-widely used stroke imaging software for patient care, research, and clinical trials—helping hospitals around the world save time, money, and lives. Rapid® is the only clinically validated platform available and considered by many to be the gold standard for advanced cerebrovascular imaging.

To learn more visit www.RapidAI.com.

About RapidAI

RapidAI is the worldwide leader in advanced imaging for stroke. Based on intelligence gained over 1,000,000 scans from more than 1,600 hospitals in over 50 countries, the Rapid® platform uses artificial intelligence to create high quality, advanced images from non-contrast CT, CT angiography, CT perfusion, and MRI diffusion and perfusion scans. The Rapid imaging platform includes Rapid ICH, Rapid ASPECTS, Rapid CTA, Rapid LVO, Rapid CTP, and Rapid MRI. RapidAI also offers SurgicalPreview®, a comprehensive aneurysm management platform.

RapidAI empowers clinicians to make faster, more accurate diagnostic and treatment decisions for stroke and aneurysm patients using clinically-proven, data-driven technology. With our validated, trusted products developed by medical experts, clinicians worldwide are improving patient care and outcomes every day. For more information, visit RapidAI.com.

Contacts

Peter Evers
Natron Communications for RapidAI
(415) 524-8899
pr@RapidAI.com

RapidAI


Release Versions

Contacts

Peter Evers
Natron Communications for RapidAI
(415) 524-8899
pr@RapidAI.com

More News From RapidAI

Worldwide Leader in Cerebrovascular Imaging Unveils Expansion of First Comprehensive Stroke Analytics Solution

MENLO PARK, Calif.--(BUSINESS WIRE)--New expanded RapidAI Insights improves hospitals’ understanding of their stroke businesses, as well as patient workflow and outcomes....

RapidAI Named Exclusive Advanced Neuroimaging Partner for the WSO and SIECV Stroke Center Certification Program in Latin America

MENLO PARK, Calif.--(BUSINESS WIRE)--RapidAI has partnered with the WSO & SIECV to become the neuroimaging partner for their new Stroke Center Certification Program in Latin America....

RapidAI Breaks New Ground And Expands AI-powered Vascular Imaging Globally

SAN MATEO, Calif.--(BUSINESS WIRE)--RapidAI, the leader in advanced cerebrovascular imaging, today announced record-shattering 2020 milestones for the company and industry, as well as an expansion of its scope into the larger vascular market. As RapidAI momentum built around the world, in addition to new products, partnerships, and awards, 2020 saw the company expand from stroke to aneurysm and lay the groundwork for other vascular diseases, both acute and non-acute. The RapidAI footprint grew...
Back to Newsroom