September 1, 2010 – The first catheter to combine near-infrared (NIR) spectroscopy with intravascular ultrasound (IVUS) to characterize coronary plaque was cleared by the U.S. Food and Drug Administration (FDA).

September 1, 2010 - A new zotarolimus-eluting coronary stent using a biocompatible polymer gained CE mark and is being launched in Europe this week. The Medtronic Resolute Integrity Stent System features a novel drug-eluting coronary stent with good deliverability, the ability of the device to traverse the patient’s vasculature and reach the blockage in the heart artery.

September 1, 2010 - Z-Medica Corp., announced that it has signed an exclusive distribution agreement with Nihon-Kohden, Japan's manufacturer, developer and distributor of medical electronic equipment. The agreement allows Nihon-Kohden the exclusive right to distribute Z-Medica’s QuikClot line of hemostatic agents to hospital, military and law enforcement markets throughout Japan.

September 1, 2010 - The Certification Commission for Health Information Technology (CCHIT) in Chicago and the Drummond Group Inc.

August 30, 2010 - A system was released in Japan last week that helps guide treatment of cardiac arrhythmias by creating a 3-D cardiac map and model based on the information from electrophysiology (EP) catheters.

August 30, 2010 – According to the results of a late-breaking analysis involving more than 200 000 patients in recent clinical trials, antihypertensive treatments with renin-angiotensin system (RAS) inhibitors significantly differ in their ability to preserve lives.

August 30, 2010 – An enhanced version of the Philips iE33 xMatrix cardiac ultrasound system features a new ergonomic transducer for more efficient adult echocardiograms.

August 30, 2010 - Even though cardiac rehabilitation, a medically supervised program of services, can significantly improve the life expectancy and quality of life of people who have had a recent cardiac event, only one in five eligible patients actually receives this lifesaving and life-improving therapy.

August 20, 2010 – Health Canada granted market approval for the Medtronic Ablation Frontiers Cardiac Ablation System, a radiofrequency (RF) ablation system to treat atrial fibrillation (AF).

August 30, 2010 - The U.S. Food and Drug Administration (FDA) granted clearance for a catheter guidance system.

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