Argon Medical Devices Inc. began marketing the CelanerXT rotational thrombectomy system as a new addition to the Cleaner family of dialysis products.
The Food and Drug Administration (FDA) has granted Biotronik approval for its Entovis pacemaker system with ProMRI technology.
May 7, 2014 — Cardiotek B.V. today announced it will commence commercialization of its EP-Tracer system following the 2014 Heart Rhythm Society (HRS) annual scientific sessions in San Francisco.
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May 7, 2014 — Women face greater limits on their lifestyle and have more severe symptoms as a result of peripheral artery disease (PAD), but minimally invasive procedures used to unclog arteries are just as successful as in men. The success of procedures, such as angioplasty or stent placement, in treating women with leg PAD was revealed in a Journal of the American College of Cardiology study.
HeartWare Intl. Inc. issued a voluntary Urgent Medical Device Correction related to all HeartWare Ventricular Assist System batteries, product codes 1650 and 1650-DE.
GE Healthcare received U.S. Food and Drug Administration (FDA) clearance for its Discovery IGS 740, a new rail-free mobile angiography system with a 41x41 cm detector.
Providing exceptional cardiovascular care for patients to achieve the best possible outcomes is the number one goal for ...

The need for improved interoperability between healthcare IT systems and medical devices has been a growing problem in an increasingly integrated medical field. This is especially true in light of U.S. healthcare reform requirements, meaningful use demands and new rules requiring software integrations to receive reimbursements from the Centers for Medicare and Medicaid Services (CMS). Physicians are trained to treat patients, not to deal with IT integration issues, and many ask why they cannot access information they need from the Internet from anywhere, the same way they do on smartphones or their home computers. Until recently, this same level of connectivity has been elusive with their own hospitals’ IT systems. Over the past couple years, vendors have answered this question by launching Web-based

The past year saw the release of several new, innovative technologies to improve nuclear imaging in both positron emission tomography (PET) and single-photon emission computed tomography (SPECT).

Cardiac ultrasound technology has advanced to keep up with several trends. These include improved workflow for greater efficiency, expanded use of qualification metrics, expanded use of 3-D echo to speed exam times and improve operator reproducibility, and expanded use of 3-D transesophageal echo (TEE) to aid guidance in the growing area of transcatheter structural heart procedures. Here are a few examples of how the newest technology is addressing these trends.
Cardiac positron emission tomography (PET) is growing in popularity among cardiologists because it provides the ability ...
May 6, 2014 — Medtronic announced the first U.S. implant of the Evera MRI SureScan implantable cardioverter-defibrillator (ICD) system, following U.S. Food and Drug Administration (FDA) approval for its investigational device exemption (IDE) application and pivotal clinical trial protocol.

May 6, 2014 — Google Glass and its potential to improve patient care will be the focus of a first-of-its-kind special session at the 2014 Society for Cardiovascular Angiography and Interventions (SCAI) scientific sessions in Las Vegas.

The American College of Cardiology (ACC) annual meeting is a key event where vendors launch new cardiology technologies. After walking the entire expo floor at ACC.14, these are my choices for some of the most innovative new technologies that were on display.
When performing radiofrequency (RF) ablation to treat cardiac arrhythmia, medical professionals must balance the safety ...

May 6, 2014 — Siemens Healthcare announced the U.S. Food and Drug Administration (FDA) has cleared the Artis one angiography system, optimized for broad clinical utilization. The Artis one is designed for routine interventions, including revascularizations of peripheral vessel occlusions, functional tests of dialysis shunts in patients with kidney failure, diagnostic or minimally invasive angiographic treatment of narrowed coronary arteries, and pacemaker implantations.
The fine print in the new Medicare legislation now mandates the use of CDS software to show tests and procedures ordered meet AUC set by medical societies in order to get full Medicare/Medicaid reimbursement.
May 6, 2014 — The National Lipid Association (NLA) recently convened an expert panel to examine various aspects of statin safety and statin tolerance. Results of the symposium findings are published this month in the Journal of Clinical Lipidology, addressing six specific statin-related safety issues including the effects of statins on cognition, diabetes risk, liver function, muscle symptoms and interactions with other drugs, and statin intolerance.