News
July 30, 2007 – The FDA gave Cook Medical, a developer of IVC filters, clearance for a permanent indication for its newest vena cava filter, Celect, which is designed to offer physicians a tool for minimizing the risk of blood clots and pulmonary embolism in their patients.
July 29, 2007
News
July 27, 2007 - Vascular disease frequently shows no symptoms until it is at such an advanced stage that it is difficult ...
July 26, 2007
Technology
July 27, 2007 - Medicomp Inc., a wholly owned subsidiary of United Therapeutics Corporation, recently introduced ...
July 26, 2007Sponsored Content
Feature | Information Technology
Providing exceptional cardiovascular care for patients to achieve the best possible outcomes is the number one goal for ...
March 21, 2024News
July 27, 2007 - Medicomp Inc., a wholly owned subsidiary of United Therapeutics Corporation, recently introduced ...
July 26, 2007News
July 27, 2007 – Cardiac Science Corp., a cardiac monitoring and defibrillation products company, received Frost & ...
July 26, 2007News
July 26, 2007 - CardiacAssist Inc., a Pittsburgh-based medical device company, announced it has completed the 1000th ...
July 25, 2007Sponsored Content
Feature | Cardiac Imaging
Cardiac positron emission tomography (PET) is growing in popularity among cardiologists because it provides the ability ...
March 05, 2024News
July 26, 2007 - St. Jude Medical Inc. announced that the U.S. FDA cleared the ACross Transseptal Access System, a device ...
July 25, 2007News
July 26, 2007 - St. Jude Medical Inc. announced that the FDA has granted clearance for the 7F Proxis Embolic Protection ...
July 25, 2007News
July 25, 2007 – Using 64-slice coronary CT angiography as a diagnostic test poses a substantial risk of developing ...
July 24, 2007Sponsored Content
Blog
When performing radiofrequency (RF) ablation to treat cardiac arrhythmia, medical professionals must balance the safety ...
December 11, 2023News
July 25, 2007 - Merit Medical Systems Inc., a manufacturer and marketer of proprietary disposable devices used primarily in cardiology and radiology procedures, announced that it has received notification from the FDA of 510(k) clearance for the Prelude sheath introducer system for transradial applications.
July 24, 2007News
July 25, 2007 – According to a study published in the July 25 issue of JAMA, high-risk patients with hypertrophic ...
July 24, 2007News
July 25, 2007 - Teleflex Incorporated, a diversified company expanding medical technology business, and Arrow ...
July 24, 2007Sponsored Content
Case Study | Hemodynamic Monitoring Systems
Change Healthcare Cardiology Hemodynamics is an integrated hemodynamic monitoring system for monitoring vital signs and ...
November 14, 2023News
July 25, 2007 - St. Jude Medical, Inc. announced the first patient implant in its clinical trial of Trifecta, a new ...
July 24, 2007News
July 25, 2007 - Researchers have confirmed that six new genetic variants increase the likelihood of developing coronary ...
July 24, 2007News
July 25, 2007 – Multidetector computed tomography (MDCT) angiography is highly accurate in depicting intracranial ...
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