The FDA cleared CryoLife’s CryoValve SG pulmonary human heart valve processed with the company’s proprietary SynerGraft ...
May 13, 2008 – The FDA approved changes to the U.S. product label for DEFINITY Vial For (Perflutren Lipid Microsphere) ...
The FDA cleared GE Healthcare’s new LightSpeed CT750 HD, said to be the world’s first high definition CT scanner that ...
Providing exceptional cardiovascular care for patients to achieve the best possible outcomes is the number one goal for ...
The FDA granted 510(k) clearance for the AIGISRX CRMD Anti-Bacterial Envelope by Tyrxpharma, a cardiac rhythm medical ...
May 13, 2008 - Edwards Lifesciences unveiled a new software upgrade that allows greater flexibility to trend and analyze ...
Abbott Vascular’s HI-TORQUE WHISPER guidewire is designed to offer a higher level of support to facilitate device ...
Cardiac positron emission tomography (PET) is growing in popularity among cardiologists because it provides the ability ...
The Edwards Lifesciences unveiled a new software upgrade that allows greater flexibility to trend and analyze the ...
May 13, 2008 – Spectranetics’ excimer laser sheath safely and effectively assists removal of pacing and defibrillator leads, according to the study, “Large, Single-catheter, Single-operator Experience with Transvenous Lead Extraction: Outcomes and Changing Indications,” featured in the April issue of HeartRhythm.
The FDA cleared for marketing a new automated version of diaDexus’ proprietary PLAC Test, an automated immunoassay designed to run on common existing laboratory equipment, including clinical chemistry analyzers from Hitachi, Roche/Hitachi and Olympus, expanding the number of clinical labs and physician offices that are able to offer the PLAC Test.
When performing radiofrequency (RF) ablation to treat cardiac arrhythmia, medical professionals must balance the safety ...
TomTec Imaging Systems recently announced that its new CardioArena, the network and imaging solution for cardiology ...
May 13, 2008 – Echoserve launched an online portal designed to facilitate the research, purchase and sale of diagnostic ...
Northeast Monitoring received clearance from the FDA to sell its DR200 Series devices with its automatic atrial ...
Change Healthcare Cardiology Hemodynamics is an integrated hemodynamic monitoring system for monitoring vital signs and ...
Boston Scientific Corp. said the FDA approved three products in its Cardiac Rhythm Management business, including the ...
May 9, 2008 – The Centers for Medicare and Medicaid Services (CMS) issued its final National Coverage Decision (NCD) to ...
May 9, 2008 - The FDA cleared Boston Scientific's ALTRUA family of pacemakers, a day after the European approval of ...