October 14, 2011 — GE Healthcare received U.S. Food and Drug Administration (FDA) clearance of the Discovery MR750w wide bore 3.0T system with GEM (Geometry Embracing Method) suite of coils.

October 14, 2011 – CardioFocus Inc., developer of the HeartLight endoscopic ablation system (EAS) for the treatment of atrial fibrillation (AF), announced that its HeartLight EAS was used to achieve successful acute pulmonary vein (PV) isolation and restore sinus rhythm in a persistent AF patient during a live case at the Venice Arrhythmias 2011 conference, Oct. 9-12 in Venice, Italy.

October 14, 2011 — The American Society of Echocardiography (ASE) is preparing a guideline document on using strain echocardiography to evaluate cancer patients for early signs of cardiac toxicity due to their medical treatments. The group has also funded a research study to enhance identification of patients who are at risk.


A U.S. Food and Drug Administration (FDA) review panel has given its unanimous recommendation for the market approval of the Zilver PTX stent. It is the first device of its kind on several fronts to go before FDA review. It is the first drug-eluting stent (DES) for peripheral leg vessels, the first self-expanding DES and the first DES that does not use a polymer to load and elute its drug.

October 12, 2011 – The Logiq S8 portable ultrasound system from GE Healthcare fits easily into small exam rooms, can be rolled to where it is needed and provides images across a variety of clinical areas including abdominal, musculoskeletal, breast, vascular and cardiology.

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