November 13, 2007- There is significant underutilization of many guideline-indicated life-saving medical and device therapies for heart failure (HF) patients, according to the Registry to Improve the Use of Evidence-Based Heart Failure Therapies in the Outpatient Setting (IMPROVE HF) study.
November 13, 2007 - Stereotaxis Inc. announced the first atrial fibrillation procedures performed with its partnered ...
November 8, 2007 – Cordis Europe has signed a deal with Volcano Europe, a developer and manufacturer of intravascular ...
Cardiac PET/CT represents a major advancement in cardiovascular diagnostics, offering significant clinical and ...
November 13, 2007 - Bayer HealthCare Pharmaceuticals Inc., a leader in diagnostic imaging, has been awarded a three-year ...
November 13, 2007 – ImaRx Therapeutics Inc. and Philips will collaborate to evaluate Philips ultrasound technology as ...
St. Jude Medical Inc. announced FDA approval of its first radiofrequency (RF) wireless devices to treat patients with heart failure and with potentially lethal heart arrhythmias.
SPONSORED CONTENT — Studycast is a comprehensive imaging workflow system that allows healthcare professionals to work ...
Q-Stress, the eighth generation stress system from Cardiac Science Inc., is built on a Microsoft Windows XP Professional ...
Toshiba’s upgraded Xario XG scanner reportedly allows for clearer image quality, expanded field-of-view imaging and ...
Terumo Interventional Systems recently released its Runthrough NS Coronary Guidewire in the U.S. market for use in percutaneous transluminal coronary angioplasties (PTCA), as the company expands its position in the coronary market.
Providing exceptional cardiovascular care for patients to achieve the best possible outcomes is the number one goal for ...
The compact ProSound Alpha 7 ultrasound system from Aloka features Directional eFLOW, which visualizes blood flow ...
Cordis Corp. announced the introduction in the U.S. market of the FIRE STAR Rx PTCA Dilatation Catheter and the DURA ...
Calgary Scientific Inc. Medical Group (CSIMG) announced the receipt of FDA 510(k) clearance for its ResolutionMD Cardiac suite of applications, including Calcium Scoring and Coronary Artery Analysis.
Cardiac positron emission tomography (PET) is growing in popularity among cardiologists because it provides the ability ...
The SDU-2200Pro ultrasound scanner from Shimadzu is said to deliver higher quality ultrasound images due to a digital ...
Concentric Medical has obtained FDA 510(k) clearance for its Merci L6 Retriever, a device that restores blood flow to ischemic stroke patients. The Merci Retriever is designed to restore blood flow by engaging, capturing and removing blood clots.
Welch Allyn’s PCE PC-based Exercise ECG Systems reportedly offer clinical features to meet any testing requirements and provide advanced database functionality for paperless storage.
November 12, 2007
