February 15, 2008 - Siemens received FDA 510(k) clearance for Artis zeego, a robotic-assisted positioning ...
Cath Lab
The catheterization lab channel includes content related to interventional technologies for coronary and peripheral artery disease (PAD). Other cath lab transcatheter device technologies covered on this page included percutaneous treatment for stroke, venous interventions, heart valves, hypertension, heart failure and percutenous coronary interventions (PCI).
February 13, 2008 - Orqis Medical Corp’s MOMENTUM Trial Abstract was accepted for a late breaking clinical trial ...
February 13, 2008 - Nfocus Neuromedical Inc. announced that the company has received CE mark approval for the CardioVasc ...
Adjustable parameters on the ACIST® CVI® Contrast Delivery System include, flow rate, volume, pressure limit, rise time ...
February 12, 2008 - Boston Scientific Corp. reported that a U.S. District Court jury in Marshall, TX, has reached a ...
February 12, 2008 – KLAS named Philips the KLAS General Market Software Category Leader for Cardiology Reporting & ...
February 12, 2008 – The FDA, National Heart Lung & Blood Institute (NHLBI) and National Science Foundation, are ...
As medical advancements continue to push the boundaries of what is possible in the field of structural heart ...
February 11, 2008 - Boston Scientific Corp. today announced that the first patient has been enrolled in its PROENCY ...
February 11, 2008 – Medrad Inc. today said it entered into a definitive merger agreement to acquire Possis Medical ...
February 11, 2008 – A new minimally invasive vascular occlusion device designed to close a patent ductus ...
While the current positive revolution in percutaneous coronary intervention (PCI) practice has been made possible by the ...
A third round of software enhancements has been made to the iLab System 1.3, an ultrasound imaging system ...
February 11, 2008 - The first patient has enrolled in the PROENCY (PROMUS, Endeavor and Cypher) European registry ...
February 8, 2008 - The FDA granted Volcano Corp. 510(k) clearance for its s5-Revo and s5-FFR (fractional flow ...
During cardiology fellowship, my institution had a hand manifold system. I found it difficult to use at times, and it ...
February 7, 2008 - Volcano Corp. said the FDA cleared the s5-Revo and s5-FFR (fractional flow reserve) options, enabling ...
February 8, 2008 - The FDA granted Volcano Corp. 510(k) clearance for its s5-Revo and s5-FFR (fractional flow ...
February 7, 2008 - Tryton Medical Inc.’s Side Branch Stent obtains CE Mark approval based on results in the Tryton ...