Itamar-Medical announced that the American Medical Association (AMA) has awarded a Current Procedure Terminology (CPT) Category III reimbursement code to a test performed by its EndoPAT proprietary device.
Abbott announced that it has entered into an agreement to purchase IDEV Technologies, a privately held company focused on developing next-generation medical devices for use by interventional radiologists, vascular surgeons and cardiologists. Under the terms of the agreement, Abbott will acquire all outstanding equity of IDEV Technologies for $310 million net of cash and debt.
July 18, 2013 — Two reports from AmericanEHR Partners, based on a survey of nearly 1,400 physicians, suggest that tablets are of greater use for clinical purposes than smart phones.
Providing exceptional cardiovascular care for patients to achieve the best possible outcomes is the number one goal for ...
July 18, 2013 — In a study of more than 2,000 adults, researchers found that two MRI (magnetic resonance imaging) measurements of the abdominal aorta — the amount of plaque in the vessel and the thickness of its wall — are associated with future cardiovascular events, such as a heart attack or stroke. Results of the study are published online in the journal Radiology.
July 18, 2013 — Boston Scientific Corp. has received U.S. Food and Drug Administration (FDA) 510(k) clearance and CE mark approval for the Guidezilla guide extension catheter.
Welch Allyn announced the availability of two connectivity-ready electrocardiograph devices in the United States. The Welch Allyn CP 150 offers flexible report formatting, intuitive design and functionality in addition to administering patient tests and managing information via a touch screen, color display. The Welch Allyn CP 50 offers the speed and power of a fully-featured ECG in a compact, portable size. Designed for use in settings where flexibility and efficiency are of utmost importance, both devices administer patient tests at the push of a button. Each can also interface with the Welch Allyn CardioPerfect Workstation to connect, manage and share patient information.
Cardiac positron emission tomography (PET) is growing in popularity among cardiologists because it provides the ability ...
The first-ever presentation at a medical conference using hologram technology instead of traditional video projection screen took place July 1 at the American Society of Echocardiography’s (ASE) 2013 scientific sessions. The innovative presentation was used to drive home the advances in technology that are going to completely reshape cardiac ultrasound and medical imaging over the next few years.
ImaCor Inc. announced the implementation of the 24/7 hTEE Clinical Support Program.
American Society of Echocardiography (ASE) President Benjamin Byrd III, M.D., FASE, explains some of the recent trends ...
When performing radiofrequency (RF) ablation to treat cardiac arrhythmia, medical professionals must balance the safety ...
DAIC Editor Dave Fornell highlights some of the biggest trends and most innovative technology discussed during the ...
July 15, 2013 — Leonhardt Ventures and Core Manufacturing LLC have announced a new partnership to manufacture and bring to market a lineup of medical technologies.
July 15, 2013 — Janssen Research & Development LLC announced the U.S. Food and Drug Administration (FDA) has issued a complete response letter for the supplemental new drug application (sNDA) for Xarelto (rivaroxaban) to reduce the risk of stent thrombosis in patients with acute coronary syndrome (ACS).
Change Healthcare Cardiology Hemodynamics is an integrated hemodynamic monitoring system for monitoring vital signs and ...
Shore University Medical Center is one of only a handful of hospitals in the country offering the recent U.S. Food and Drug Administration (FDA)-approved Lariat Suture Delivery Device procedure. Electrophysiologists and interventional cardiologists perform this innovative procedure to help prevent stroke in patients who suffer from atrial fibrillation and are unable to take blood thinners.
The lag in FDA approval time for major medical innovations has come increasing concerns about the ability of the United States to remain at the forefront of research, especially in light of stringent FDA policies regarding clinical trials and device approval.
July 12, 2013 — A Chicago native living in southern California was the first patient at Scripps Health to receive a MitraClip as part of the clinical outcomes assessment of the MitraClip Percutaneous Therapy for High Surgical Risk Patients (COAPT) trial.