March 21, 2008 - Cordis Corp. has received 510(k) marketing clearance from the FDA for the S.M.A.R.T. Nitinol Stent Transhepatic Biliary System for lengths of 120 mm and 150 mm, the company reported at the 33rd Annual Scientific Meeting of the Society of Interventional Radiology (SIR) meeting.
March 21, 2008 — The Drug Information Association (DIA) will host an educational forum in conjunction with the FDA and ...
March 21, 2008 – A central Ohio man has become the first person in the U.S., and only the 16th worldwide, to receive a ...
Providing exceptional cardiovascular care for patients to achieve the best possible outcomes is the number one goal for ...
March 18, 2008 - Cardinal Health and GE Healthcare penned a deal to broaden the availability of GE Healthcare's Myoview ...
March 21, 2008 - The FDA gave conditional approval to PLC Systems to begin enrollment in a U.S. pivotal trial to study ...
GE will highlight a new design concept for its Vivid S5 cardiovascular ultrasound system, combining features from its ...
Cardiac positron emission tomography (PET) is growing in popularity among cardiologists because it provides the ability ...
The LightSpeed VCT CT scanner for cardiac imaging reportedly reduces a patient�s radiation exposure by up to 70 ...
The Vivid S6 signature class cardiovascular ultrasound system reportedly combines strong performance and excellent image ...
The LIFEPAK 12 defibrillator/monitor offers full-featured defibrillation and industry-standard monitoring for emergency services and hospitals. It utilizes ADAPTIV biphasic technology and combines semi-automatic and manual defibrillation. The 12 features capnography, external pacing, 12-lead electrocardiography and enhanced monitoring capabilities.
When performing radiofrequency (RF) ablation to treat cardiac arrhythmia, medical professionals must balance the safety ...
March 20, 2008 - ARUP Laboratories and the University of Utah's Department of Pathology have released ARUP Consult version 2.3, a free laboratory test selection support tool for PDA devices that includes more than 1,500 lab tests categorized into disease-related topics, including clinical background information, test ordering suggestions and concise diagnostic advice.
The Vivid e adds a fully integrated, three-connector, docking cart, creating a true hybrid system with the power of ...
The LIFEPAK 1000 defibrillator/monitor is the most rugged defibrillator ever designed by Physio-Control, with an IP55 rating. ADAPTIV biphasic technology provides a range of energy up to 360 joules, and an upgradeable platform. The 1000 is equipped with cprMAX technology, enabling care providers to change protocols as standards of care evolve.
Change Healthcare Cardiology Hemodynamics is an integrated hemodynamic monitoring system for monitoring vital signs and ...
March 18, 2008 - McKesson reports that it is unveiling two new Horizon Cardiology products for the cath lab, including ...
McKesson has released a new Horizon Cardiology product for the cath lab, the Holding Area Charting, designed to simplify and expedite information flow in the cath lab, increase data accuracy by minimizing duplication and strengthen the facility’s commitment to patient safety.
March 18, 2008 - Northeast Monitoring Inc. released LX Sleep, a software product that reportedly detects OSA from data collected during a simplified, overnight, at-home, patient hookup to its OxyHolter product, as the company plans to launch its product line worldwide.