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Result: Searchterm 'Food and Drug Administration' found in 73 news
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FDA Clears Compressed Sensing MRI Acceleration Technology From Siemens Healthineers
'''''Siemens Healthineers has announced that the Food and Drug Administration (FDA) has cleared the company's revolutionary Compressed Sensing technology, which slashes the long acquisition ...'
Tuesday, 21 February 2017   by www.healthimaging.com
IRADIMED CORPORATION Receives FDA Clearance for MRI Compatible IV Infusion Pump
'''''IRADIMED CORPORATIONÂ (NASDAQ:IRMD), today announced that it received U.S. Food and Drug Administration (FDA) 510(k) clearance for its MRidium 3860+ magnetic resonance imaging (MRI) compatible ...'
Monday, 19 December 2016   by www.econotimes.com
BIOTRONIK Announces FDA Approval of MR Conditional Cardiac Resynchronization Defibrillators
'''''BIOTRONIK, a leader in cardio- and endovascular medical technology, today announced Food and Drug Administration (FDA) approval of Iperia ProMRI HF-T, a cardiac resynchronization defibrillator ...'
Tuesday, 3 May 2016   by www.prnewswire.com
FDA Approves First MRI-Safe CRT Defibrillators
'''''The U.S. Food and Drug Administration (FDA) approved on Feb. 5 Metronic's Amplia MRI Quad CRT-D SureScan and Compia MRI Quad CRT-D SureScan devices for the treatment of heart failure (HF). Both cardiac resynchronization therapy defibrillators (CRT-Ds) ...'
Tuesday, 9 February 2016   by www.acc.org
Siemens Announces FDA Clearance of Magnetom Amira MRI Scanner
'''''Siemens Healthcare announced that the U.S. Food and Drug Administration (FDA) has cleared the Magnetom Amira 1.5 Tesla magnetic resonance imaging (MRI) system. Boasting new 'Eco-Power' technology that enables significant power savings in standby ...'
Thursday, 21 January 2016   by www.itnonline.com
FDA Approves BIOTRONIK Iperia ICD Systems with Full-Body ProMRI Technology
'''''BIOTRONIK, a leading manufacturer of cardiovascular medical technology, announced today that it has received Food and Drug Administration (FDA) approval for use of its latest family of implantable cardioverter defibrillator (ICD) systems with magnetic ...'
Tuesday, 22 December 2015   by www.businesswire.com
Mallinckrodt (MNK) Announces FDA Clearance of INOmax DSIR Plus MRI Device
'''''Mallinckrodt (NYSE: MNK) announced that the U.S. Food and Drug Administration (FDA) has cleared INOmax DSIR Plus MRI device for delivery of INOMAX (nitric oxide) for inhalation during MRI procedures. The INOmax DSIR Plus MRI delivery system is ...'
Monday, 16 November 2015   by www.streetinsider.com
Medtronic First to Receive FDA Approval for MR-Conditional Implantable Cardioverter Defibrillator System
'''''Medtronic plc MDT, -0.36% today announced that it has received the first U.S. Food and Drug Administration (FDA) approval for an implantable cardioverter defibrillator (ICD) system for use with magnetic resonance imaging (MRI) scans. The Medtronic Evera ...'
Monday, 14 September 2015   by www.marketwatch.com
FDA Examines Whether MRI Drugs Accumulate in Brain Tissue
'''''The Food and Drug Administration announced today it is investigating the risk of brain deposits for patients who are given repeated MRIs using imaging drugs that contain a heavy metal. The FDA did not announce any label changes for the nine medicines ...'
Monday, 27 July 2015   by www.propublica.org
FDA to Replace 17-Year-Old Guidance for MRI Premarket Notifications
'''''The US Food and Drug Administration (FDA) is seeking input as it begins to draft a new guidance intended to help makers of magnetic resonance diagnostic devices (MRDDs) complete premarket notification 510(k) applications.BackgroundAfter scientific ...'
Tuesday, 14 July 2015   by www.raps.org
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