Technology

Baxter Healthcare Corp. received FDA 510(k) clearance for its needleless V-Link Luer-activated device (LAD), an IV ...

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Power Medical Interventions Inc. said the FDA cleared its intelligent iDrive surgical devices, which includes a suite of ...

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The SafeSeal Hemostasis Patch topical wound dressing is designed to decrease the time it takes to control bleeding from the puncture made into a blood vessel to perform an endovascular procedure.

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Feature | Dave Fornell

February 2008 - The traditional hospital cleaning methods of wiping down surfaces and mopping floors are now being ...

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Siemens Medical Solutions received FDA 510(k) clearance for a 1.5T magnetic resonance imaging (MRI) system that is ...

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February 20, 2008 - Philips Medical Systems features at HIMSS 2008 enhancements to its speech recognition solution ...

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W. L. Gore & Associates (Gore) announced that the FDA granted approval for the use of GORE HELEX Septal Occluder with a modified catheter delivery system indicated for the transcatheter closure of atrial septal defect (ASD), providing a percutaneous ASD closure solution for very young patients.

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February 20, 2008 - At HIMSS 2008, Siemens Healthcare will emphasize its image data management solutions for radiology ...

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Toshiba America Medical Systems Inc. recently introduced its Infinix VF-i/SP X-ray system, a universal cardiovascular ...

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The ACUSON X300 works to provide compact, portable color Doppler solutions for adult, pediatric, OR, EP and ...

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February 19, 2008 – The American College of Cardiology (ACC) urges the medical community to oppose cuts to medical ...

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February 19, 2008 - Boston Scientific Corp. closed the sale of its Fluid Management and Venous Access businesses to ...

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February 19, 2008 - A new study released today found pending congressional legislation seeking the mandatory disclosure ...

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February 19, 2008 - Among patients with acute myocardial infarction (AMI), prior statin therapy is associated with better perfusion after primary angioplasty of the infarct-related artery, according to a report in the January 15 issue of the American Journal of Cardiology.

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February 19, 2008 – The first CE certified Nobori Drug-Eluting Coronary Stent System was successfully implanted in Europe, as Terumo Corp. is poised to expand the product from spring 2008 to more than 20 countries in Europe, Asia, New Zealand and Africa.

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