January 5, 2011 — The U.S. Food and Drug Administration (FDA) has given clearance for Medic Vision Ltd. to market its SafeCT product in the United States. SafeCT processes and enhances images spanning a broad range of clinical applications acquired on a wide variety of computed tomography (CT) scanners.

January 4, 2011 - The Centers for Medicare and Medicaid Services (CMS) and the Office of the National Coordinator for Health Information Technology (ONC) yesterday announced the availability of registration for the Medicare and Medicaid electronic health record (EHR) reimbursement incentive programs.

January 4, 2010 – The U.S. Food and Drug Administration (FDA) has released an update of what medical devices it expects to be developed and brought to market within the next 10 years.

January 4, 2011 - The Office of the National Coordinator for Health Information Technology (ONC) has issued a final rule to establish the permanent certification program for health information technology.

January 4, 2011 – An automated, digital blood pressure device is now available in the United States and Canada. The Connex ProBP 3400, from Welch Allyn, fits in the palm of the hand and provides a portable option for capturing reliable blood pressure readings in virtually any hospital or primary care environment.

January 3, 2011 — A portable viewing application that interfaces with an existing RIS/PACS/cardiology PACS for access to images and reports has been introduced.

January 3, 2011 – Two new classes — “Advanced Computed Tomography (CT) Imaging for Technologists” and “Advanced Non-Contrast Magnetic Resonance Angiography (MRA)” — are being offered to educate technologists on the latest applications available with their Toshiba technology. They are offered by Toshiba America Medical Systems Inc.’s Education Center in Irvine, Calif.

January 3, 2011 – ev3, a Covidien company, has initiated a voluntary recall of specific lots of the NanoCross .014-inch Over-the-wire (OTW) peripheral transcatheter angioplasty (PTA) dilatation catheter due to the potential for the catheter shaft to crack or break during use.

January 3, 2011 – Arrow International, a division of Teleflex Medical, issued a class I recall, advising customers to immediately discontinue use of its Ultra 8 French intra-aortic balloon pump (IABP) catheters.

December 29, 2010 - Research on reducing risks, improving medical treatment and improving lifestyle behaviors to fight the battle against heart disease and stroke are among the key scientific findings that make up this year's top cardiovascular and stroke research recognized by the American Heart Association/American Stroke Association.
Subscribe to
© Copyright Wainscot Media. All Rights Reserved.
Subscribe Now