Technology

The FDA cleared for marketing the Reliant, a portable cardiac output monitor that provides a noninvasive window to cardiac and hemodynamic function.

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InTouch Technologies Inc. offers StrokeRESPOND to extend the functionality of its telemedicine, Remote Presence robotic technology for stroke experts.

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Northeast Monitoring’s DR200/HE is a combination 14-day Holter plus 30-day Event recorder integrated into a single unit that is designed for deployment to patients in either 'Holter' or 'Event' mode.<...

The ACUSON SC2000 volume imaging ultrasound system acquires nonstitched, real-time full-volume 3D images of the heart in one single heart cycle.
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The Welch Allyn Holter System is a reportedly easy-to-use software and recording device that helps caregivers detect abnormalities in a patient’s heart rhythm over an extended period of time....

The FDA cleared GE Healthcare’s new LightSpeed CT750 HD, said to be the world’s first high-definition CT scanner that produces images 100 times faster with up to 33 percent greater detail through the ...

3M Health Care offers the 3M Filtro 1900 tie-on duckbill surgical mask that incorporates proprietary filtration media and a rayon outer layer for increased breathability and comfort.

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IntelliDOT Corp. received FDA 510(k) clearance for the IntelliDOT Blood Product Administration (IntelliDOT BPA) for commercial sale.

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The TandemHeart System ventricular assist device by CardiacAssist assists heart failure patients survive both heart attacks and high risk procedures, while providing versatility to physicians in choos...

Lexiscan (regadenoson) injection is an A2A adenosine receptor agonist for use as a pharmacologic stress agent in radionuclide myocardial perfusion imaging (MPI) in patients unable to undergo adequate ...

The Philips BrightView XCT integrates Philips BrightView SPECT in a coplanar design with advanced flat-detector X-ray CT technology to acquire low dose, high resolution CT images and to improve regist...

OrbusNeich's Scoreflex coronary dilatation catheter, which is only CE Mark approval, but not yet FDA cleared, is a new product that extends OrbusNeich's balloon catheter portfolio.

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