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MRI News Service:
'Food and Drug Administration' p7 |
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| Result: Searchterm 'Food and Drug Administration' found in 73 news | | Result Pages | | More Results:  Database (9) |
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 | | | '''''IMRIS Inc. (TSX: IM) ('IMRIS' or the 'Company') today announced that it has received 510(k) clearance from the US Food and Drug Administration (FDA), permitting the Company to market its newest products, IMRISNV and IMRIScardio in the United ...' | | Tuesday, 8 September 2009 by www.reuters.com |
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| | | '''''The United States Food and Drug Administration has granted IRadimed Corporation clearance of its new MRidium 3860+ MRI Infusion System with integrated Masimo SET(R) SpO2 Monitoring. Transport to the MRI for Sedation, Critical Care, and Cardiac Patients ...' | | | Monday, 17 August 2009 by www.biospace.com | |
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| | | '''''IntroductionAt present, no disease-modifying osteoarthritis drugs (DMOADS) are approved by the FDA (US Food and Drug Administration); possibly partly due to inadequate trial design since efficacy demonstration requires disease progression in the placebo ...' | | | Friday, 24 July 2009 by 7thspace.com | |
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| | | '''''KALAMAZOO -- A medical-technology company that established its headquarters in Kalamazoo last year has received approval to begin using a device it invented to treat brain tumors previously considered to be inoperable. The U.S. Food and Drug ...' | | | Thursday, 14 May 2009 by www.mlive.com | |
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| | | '''''WASHINGTON, Dec. 24 (Xinhua) -- The U.S. Food and Drug Administration on Wednesday approved Vasovist Injection, the first contrast imaging agent for use in patients undergoing magnetic resonance angiography, or MRA, a minimally invasive test for ...' | | | Thursday, 25 December 2008 by news.xinhuanet.com | |
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| | | '''''Mercury Computer Systems of Chelmsford said today that its Visage unit received Food and Drug Administration clearance to sell a new medical imaging unit. The company's Visage CS 3.1 performs a range of imaging functions, including CAT scans and ...' | | | Monday, 15 December 2008 by www.boston.com | |
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| | | '''''MINNEAPOLIS – Feb. 1, 2008 –Marking a major development in the field of interventional cardiology, Medtronic, Inc. (NYSE: MDT), announced today that it has received approval from the U.S. Food and Drug Administration (FDA) for the Endeavor® ...' | | | Friday, 1 February 2008 by wwwp.medtronic.com | |
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| | | '''''SUNNYVALE, Calif., Dec. 21 /PRNewswire-FirstCall/ -- Pharmacyclics,
Inc. (Nasdaq: PCYC) today announced that it has received a non-approvable
letter from the U.S. Food and Drug Administration (FDA) for the company's
new drug application (NDA) ...' | | | Friday, 21 December 2007 by www.prnewswire.com | |
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| | | '''''WASHINGTON (Reuters) - Certain contrast agents used in magnetic resonance imaging -- gadolinium-based products made by Bayer AG, GE and others -- will now carry the U.S. Food and Drug Administration's strongest, 'black box' warning. The FDA's ...' | | | Friday, 28 September 2007 by uk.reuters.com | |
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| | | '''''HAIFA, Israel, March 1, 2007 – InSightec Ltd. announced today that the U.S. Food and Drug Administration (FDA) has approved software that significantly speeds up the treatment time of the company’s ExAblate 2000 Magnetic Resonance guided Focused ...' | | | Thursday, 1 March 2007 by www.insightec.com | |
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