May 29, 2007 — The FDA has cleared the CORDIS ENTERPRISE Vascular Reconstruction Device and Delivery System under the Humanitarian Device Exemption — it is used with embolic coils for the treatment of intracranial aneurysms. It consists of a self-expanding stent and a delivery system. The stent serves as a scaffold for embolic coils to prevent herniation of the coils into the parent vessel.
May 29, 2007 — Abbott announced positive results last week from ABSORB, the world’s first clinical trial evaluating the ...
May 23, 2007 — InspireMD has announced this week the enrollment of 19 patients in its First in Man study in a ...
Providing exceptional cardiovascular care for patients to achieve the best possible outcomes is the number one goal for ...
May 22, 2007 — Luna Innovations has announced it has received a market clearance letter in response to its 510(k) ...
May 23, 2007 — MicroMed Cardiovascular Inc. has announced that on Monday, May 14, 2007, doctors at Freeman Hospital in ...
May 23, 2007 — MedicalCV Inc. has announced that the United States Patent and Trademark Office ("USPTO") has issued ...
Cardiac positron emission tomography (PET) is growing in popularity among cardiologists because it provides the ability ...
May 23, 2007 — XTENT Inc. announced positive six-month follow-up data from the CUSTOM II clinical trial, which assessed ...
May 21, 2007 — Sanofi-aventis has announced that the FDA has approved a supplemental New Drug Application (sNDA) for the ...
May 21, 2007 — OrbusNeich announced today it has received CE Mark approval for three interventional cardiology products ...
When performing radiofrequency (RF) ablation to treat cardiac arrhythmia, medical professionals must balance the safety ...
May 21, 2007 — Findings presented last week during the annual meeting of the Heart Rhythm Society in Denver indicate a common stress test, using GE Healthcare’s latest algorithm for the measurement of T-wave Alternans (TWA), can be useful in predicting sudden cardiac death, even in those without a previous heart attack or symptoms of heart failure.
May 18, 2007 — Inverness Medical Innovations Inc. and Biosite Inc. have announced the companies have entered into a ...
May 18, 2007 — CoreValve has announced that it has received CE Mark approval of its CoreValve Percutaneous ReValving ...
Change Healthcare Cardiology Hemodynamics is an integrated hemodynamic monitoring system for monitoring vital signs and ...
May 18, 2007 — Hansen Medical Inc. said Thursday it obtained approval in the European Union for its Sensei robotic ...
May 18, 2007 — Medicure, a biopharmaceutical company focused on the research, development and commercialization of novel ...
May 18, 2007 — According to a report published Thursday in the Wall Street Journal and posted on UPI, the number of ...