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March 21, 2008 - The FDA gave conditional approval to PLC Systems to begin enrollment in a U.S. pivotal trial to study ...

Home March 20, 2008
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March 20, 2008 – The number of CT procedures performed continues to grow despite a slow down in CT system purchases from ...

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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.

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March 21, 2008 — The Drug Information Association (DIA) will host an educational forum in conjunction with the FDA and ...

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March 21, 2008 – A central Ohio man has become the first person in the U.S., and only the 16th worldwide, to receive a ...

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Technology

The Vivid S6 signature class cardiovascular ultrasound system reportedly combines strong performance and excellent image ...

Home March 19, 2008
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Technology

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.

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Technology

The Vivid e adds a fully integrated, three-connector, docking cart, creating a true hybrid system with the power of ...

Home March 19, 2008
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Technology

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.

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Technology

GE will highlight a new design concept for its Vivid S5 cardiovascular ultrasound system, combining features from its ...

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Technology

The LightSpeed VCT CT scanner for cardiac imaging reportedly reduces a patient�s radiation exposure by up to 70 ...

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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.

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March 18, 2008 – The FDA gave AtriCure’s Coolrail linear ablation pen 510(k) clearance for the ablation of cardiac ...

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March 18, 2008 – Northeast Monitoring received clearance from the FDA to sell its DR200 Series devices with its ...

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Bacchus Vascular Inc. has developed a catheter-based device, the Trellis-8 infusion catheter, which disperses ...

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