LONDON — Research group IMEC and Terepac Corp. (Waterloo, Canada) are joining forces to develop a wireless ECG system within the Human++ Program at IMEC's Holst Centre in Eindhoven, the Netherlands.

The US Food and Drug Administration (FDA) has granted 510(k) regulatory clearance to the Curvus Arrhythmia Monitoring Device (C-AD), a wireless-enabled and continuous tracker of real-time ECG readings ...

Clario has obtained 510(k) clearance from the US Food and Drug Administration (FDA) for its SpiroSphere with the integrated wireless COR-12 electrocardiogram (ECG) device. The clearance enables the ...

New York-based Peerbridge Health announced that its wireless device, dubbed the Peerbridge Cor System, is the latest ECG device to receive 510(k) clearance from the FDA. According to the company, the ...

An interview with Dr. Angelo Acquista, Founder of Peerbridge Health, conducted by April Cashin-Garbutt, MA (Cantab). What is the vision behind Peerbridge Health? Our vision is to remove all wires ...

With the FDA 510(k) clearance of the COR-12 wireless ECG device now integrated with the SpiroSphere®, sponsors can conduct comprehensive respiratory trials with cardiac safety ECG collection on one ...

SANTA CLARA, Calif.--(BUSINESS WIRE)--HeartBeam, Inc. (NASDAQ: BEAT), a medical technology company focused on transforming cardiac care through the power of personalized insights, announced today that ...

At Report Ocean, our goal is to merge comprehensive industry insights with top-notch research methodologies, empowering our clients to conquer future business challenges and attain their goals. Our ...

Report Ocean published the latest research report on the “Wireless Electrocardiography (ECG) Devices Market”. In order to comprehend a market holistically, a variety of factors must be evaluated, ...

Dublin, Dec. 05, 2024 (GLOBE NEWSWIRE) -- The "ECG Equipment and Management Systems - Global Strategic Business Report" report has been added to ResearchAndMarkets.com's offering. The global market ...