St. Jude Medical Inc. says it has received FDA approval of a new cardiac rhythm management device designed to help physicians manage heart failure (HF) patients, including patients who have or may develop atrial fibrillation (AF).
A new MRI monitor to complement the Maglife product line, the Maglife light makes MRI monitoring within reach of virtually every MRI Center. It can handle all monitoring needs and is compatible with MRI scanners up to 3T.
When used in conjunction with the ev3 embolic protection device, ev3’s PROTÉGÉ RX Carotid Stent has been FDA cleared for the treatment of carotid artery disease in patients who are at high-risk for adverse events from carotid artery surgery. The cleatance was supported by the CREATE (Carotid Revascularization with ev3 Inc.
Providing exceptional cardiovascular care for patients to achieve the best possible outcomes is the number one goal for ...
VIASYS Healthcare is showcasing the launch of the MasterScreen CPX, a product that combines 40 years of CPET experience into a compact unit.
Pfizer says the FDA has approved the company’s Lipitor (atorvastatin calcium) Tablets to reduce the risk of nonfatal heart attacks, fatal and non-fatal strokes, certain types of heart surgery, hospitalization for heart failure, and chest pain in patients with heart disease — making Lipitor the first cholesterol-lowering medication to receive FDA approval for the reduction of the risk of hospit
Diagnosoft HARP is software that assists physicians in the analysis of magnetic resonance (MR) images by providing quantitative measurements and visualization of regional heart function. Based on technology from Johns Hopkins University, it’s the first FDA-cleared software designed for the analysis of tagged MR images.
Cardiac positron emission tomography (PET) is growing in popularity among cardiologists because it provides the ability ...
The NICO2 Respiratory Profile Monitor is designed to monitor the patient side of the breathing circuit. NICO2 goes beyond conventional capnography to measure breath-by-breath volumetric CO2 and takes the guesswork out of ventilation management from setup to weaning.
Rcadia Medical Imaging Ltd., an Israel-based developer of novel computer-aided diagnostic software, has received FDA clearance to market its COR Analyzer I, which assists screening of triage patients for coronary artery disease.
Exercise Tolerance Testing (ETT) is a diagnostic tool consisting of the RHE cycle, that is used in conjunction with scientifically validated exercise testing protocols to create a more accurate, sensitive and comfortable test, according to the company.
When performing radiofrequency (RF) ablation to treat cardiac arrhythmia, medical professionals must balance the safety ...
The intra-aortic balloon pump (IABP) is an minimally invasive technology designed to enhance blood flow to the heart and other organs for patients with diminished heart function.
Coronary computed tomography angiography (CCTA) has recently made significant technological and clinical advances. Submillimeter slice thickness, increased detectors and reduced acquisition times have multiplied the number of patients that can benefit from noninvasive diagnostic imaging.
Sentinel integrates the entire range of noninvasive diagnostic cardiology solutions including: ECG Exercise Testing, 12-Lead ECG, Holter Monitoring, ECG Event Recording and Ambulatory Blood Pressure Monitoring into one central data management system.
Change Healthcare Cardiology Hemodynamics is an integrated hemodynamic monitoring system for monitoring vital signs and ...
MasterScreen CPX is a complete exercise test that includes a stress ECG option. Its digital TripleV-Volume Sensor complies with ATS criteria, performs without drift and is completely insensitive to moisture. It features a lightweight design (45g), minimal resistance to airflow, dead space of 30mL and it can be used for all patient populations.
The Vanguard Dx Angiographic Catheter with patented RadiantFlow tip technology delivers contrast in a unique way. Vanguard Dx produces a “cloud” of contrast rather than a jet stream like traditional catheters. This cloud-like dispersion helps to reduce catheter whipping and enhance tip stability. The catheters are available in the 15 most common shapes and in 4F and 5F sizes.
The FDA has granted clearance to the Cordis Endovascular division of Cordis Corp. to market its PRECISE RX Nitinol Self-Expanding Stent and ANGIOGUARD RX Emboli Capture Guidewire System to treat clogged neck arteries. The approval was announced during the Arizona Heart Institute's International Congress on Endovascular Interventions in Scottsdale, AZ.