February 16, 2012 — U.S. Food and Drug Administration (FDA) granted 510(k) clearance for AngioDynamics NeverTouch Direct ...
Diagnostic and Interventional Cardiology DAIC
Diagnostic and Interventional Cardiology (DAIC) is a magazine that reaches more than 25,000 healthcare professionals in cardiology, interventional cardiology and cath labs across the United States. These influential buying team members rely on DAIC's award-winning editorial content and comparison charts as a unique research tool for specifying, recommending and approving technology/device purchases.
February 16, 2012 — Few hospitals have as much experience with the Berlin Heart pediatric ventricular assist device (VAD ...
February 16, 2012 — Siemens Healthcare received clearance from the U.S. Food and Drug Administration (FDA) for syngo Aor ...
February 16, 2012 — Aptus Endosystems Inc. a medical device company developing advanced technology for endovascular ...
February 15, 2012 — Vessix Vascular Inc., developer of a novel percutaneous radiofrequency (RF) balloon catheter ...
February 15, 2012 — Medtronic Inc. announced the start of two clinical initiatives evaluating the broader, real-world ...
Being a child of the late 1970s and 1980s, I was a big Star Wars fan. Somewhere in my basement I still have the action ...
February 6, 2012 — Vascular Solutions Inc. announced it is marketing a reprocessing service for the ClosureFAST ...
February 3, 2012 — Colibri Heart Valve received an notification it received patents for a new transcatheter heart valve ...
February 3, 2012 — Medtronic Inc. issued a statement on the results of two studies evaluating the use of the Medtronic ...
February 2, 2012 — Abiomed Inc. announced that initial clinical data from the safety study for Symphony was presented by ...
Based on my observations and those of the doctors on the Diagnostic & Interventional Cardiology Editorial Advisory Board ...
With the approval of the Sapien valve in November 2011, transcatheter aortic valve implantation (TAVI) technology is ...
Recently, the U.S. Food and Drug Administration (FDA) has approved the Edwards Sapien transcatheter heart valve for ...
January 30, 2012 — Medtronic, Inc. announced the completion of patient enrollment in the extreme risk study in its ...
February 16, 2012