Summit Doppler Systems upgraded the Vista AVS, a full-featured arterial physiologic exam system, which allows clinicians to perform the ankle brachial index (ABI) exam for the diagnosis of peripheral arterial disease (PAD) in the seated position.
St. Jude Medical said recently the FDA cleared its new delivery tools designed to give physicians greater control and precision when placing cardiac pacing leads. The CPS Duo stylet and guide wire system, the PCS Courier guide wire and the Mond stylet are all tools designed to place leads in precise positions that can be difficult to access.
The Welch Allyn Holter System is a reportedly easy-to-use software and recording device that helps caregivers detect ...
Cardiac PET/CT represents a major advancement in cardiovascular diagnostics, offering significant clinical and ...
July 9, 2008 – The American Heart Association recently issued new guidelines for computed tomography (CT) and magnetic ...
The StarClose SE Vascular Closure System is a next-generation vessel closure device engineered to enable fast and secure closure of the femoral artery access site following a catheterization procedure.
The FDA cleared for marketing the Reliant, a portable cardiac output monitor that provides a noninvasive window to ...
SPONSORED CONTENT — Studycast is a comprehensive imaging workflow system that allows healthcare professionals to work ...
July 9, 2008 - Summit Doppler Systems this week introduced a significant upgrade to the Vista AVS, a full-featured ...
InTouch Technologies Inc. offers StrokeRESPOND to extend the functionality of its telemedicine, Remote Presence robotic ...
Thoratec Corp. received FDA approval of its PMA (premarket approval) application, allowing the use of its HeartMate II LVAS (left ventricular assist system) as a bridge-to-transplantation (BTT) in patients suffering from advanced-stage heart failure.
Providing exceptional cardiovascular care for patients to achieve the best possible outcomes is the number one goal for ...
Northeast Monitoring’s DR200/HE is a combination 14-day Holter plus 30-day Event recorder integrated into a single unit ...
July 9, 2008 - Omron Healthcare Inc. released a new portable, single patient use monitor series, the HBP-T105. The new ...
The FDA cleared GE Healthcare’s new LightSpeed CT750 HD, said to be the world’s first high-definition CT scanner that ...
Cardiac positron emission tomography (PET) is growing in popularity among cardiologists because it provides the ability ...
Vascular Insights received 510(k) clearance from the FDA to market its ClariVein infusion catheter for infusion of physician-specified agents in the peripheral vasculature. ClariVein is a percutaneous, 2 2/3 Fr (0.035-inch) catheter, containing a rotating wire driven by a motor, that enhances fluid dispersion in the treatment area.
July 9, 2008 – An article in the July issue of The Journal of Clinical Hypertension indicates an increased intake in ...
The Abiomed Inc. Impella 2.5 cardiac assist device was FDA cleared in 2008 for use for partial circulatory support for periods up to six hours. The intra-aortic balloon pump (IABP) also has 510(k) clearance and approximately 110,000 are used each year in the U.S.
July 08, 2008
