Technology

August 11, 2011 – GE Healthcare announced U.S. Food and Drug Administration (FDA) clearance of Optima CT660 – a compact computed tomography (CT) system offering improvements from its predecessors in diagnostic capabilities at low dose levels. The system is designed for sustainability and ease-of-use.

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August 11, 2011 – Researchers have found more evidence supporting the role of fat around the heart in promoting atherosclerosis, according to a study published online in the journal Radiology.

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August 10, 2011 — Hospitals vary markedly when it comes to the rate at which diagnostic coronary angiography or catheterization – an invasive procedure that allows doctors to see the vessels and arteries leading to the heart – actually finds obstructive coronary artery disease (CAD) in people without known heart disease.

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August 10, 2011 – The U.S. Food and Drug Administration (FDA) has approved Abbott’s RX Herculink Elite Renal Stent System for the treatment of renal artery stenosis (narrowing of the main arteries supplying blood to the kidneys) in patients with uncontrolled hypertension (high blood pressure). Over time, narrowed kidney arteries can lead to kidney failure and increased risk of heart disease, stroke and peripheral artery disease. This approval is supported by the HERCULES (Herculink Elite Cobalt Chromium Renal Stent Trial to Demonstrate Efficacy and Safety) study, which demonstrated that RX Herculink Elite is safe and effective in patients with renal artery stenosis and uncontrolled hypertension.

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August 10, 2011 – In the 3.0 Tesla (T) magnetic resonance (MR) marketplace, patient compliance often impacts image quality and patient throughput. As the only 3.0T MR system designed to improve patient compliance and comfort while offering advanced radiology capabilities, Toshiba America Medical Systems Inc.’s new Vantage Titan 3.0T open-bore MR has received U.S. Food and Drug Administration (FDA) clearance. The new system is the only 3.0T MR offering patient-friendly features such as noise reduction, a wide and open bore, feet-first imaging and Toshiba’s proprietary contrast-free techniques.

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August 9, 2011 — Boston Scientific Corp. said the U.S. Court of Appeals for the First Circuit has affirmed the dismissal of a securities fraud case in connection with the 2004 recall of one of the company’s coronary stent systems.

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August 9, 2011 — Acist Medical Systems Inc., a Bracco Group company and provider of advanced contrast injection system technology for cardiovascular angiography, announced that its’ Contrast Delivery System has been used to help diagnose and treat 10 million patients.

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August 9, 2011 — The American Heart Association (AHA) 2011 annual scientific sessions will be held Nov. 12-16, in Orlando, Fla.

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August 8, 2011 – Edwards Lifesciences announced the global launch of the Carpentier-Edwards Physio Tricuspid Annuloplasty Ring for the treatment of tricuspid valve insufficiency. The company received both 510(k) clearance from the U.S. Food and Drug Administration (FDA) and CE mark for European sales of the device.

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August 8, 2011 — Elsevier, provider of scientific, technical and medical information products and services, announced its Braunwald's Heart Disease Practice Guides App for iPad, iPhone and iPod Touch is now available on the App Store.

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August 8, 2011, — Cambridge Heart announced that the Freeport, Maine Fire Department has applied for a federal grant to establish firefighter screenings for sudden cardiac arrest (SCA) risk using the company’s Microvolt T-Wave Alternans (MTWA) non-invasive diagnostic test.

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August 5, 2011 – New software aimed at making computed tomography (CT) safer for patients estimates the radiation risk based on age, gender and size rather than using the current “one size fits all” approach. The software program, tested on more than 6,500 scans, was introduced at the 2011 Joint Meeting of the American Association of Physicists in Medicine (AAPM) and Canadian Organization of Medical Physicists (COMP).

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August 5, 2011 — Heart failure circulatory support system maker Thoratec Corp. announced it acquired the medical business of ventricular assist device (VAD) maker Levitronix Medical. The company developed a pediatric VAD, which is currently pending U.S. Food and Drug Administration (FDA) clearance. Levitronix was purchased in a cash payment of $110 million, as well as potential future cash earnout payments of up to $40 million.

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August 5, 2011 — BridgePoint Medical Inc., a Minnesota-based medical device company, has enrolled its first patient in the Peripheral Facilitated Antegrade Steering Technique in Chronic Total Occlusions (PFAST-CTOs) study.

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August 5, 2011 — Vessix Vascular Inc. (formerly known as Minnow Medical Inc.), developer of novel percutaneous radiofrequency (RF) balloon catheter technology for peripheral leg vessels, announced it has completed a $23 million Series B preferred stock financing.

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