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Result: Searchterm 'Food and Drug Administration' found in 73 news
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FDA clears new AI-powered MRI system from Fujifilm
'''''The U.S. Food and Drug Administration has cleared a new magnetic resonance imaging system from Fujifilm, the company announced on Wednesday. The Echelon Synergy MRI machine utilizes ...'
Thursday, 24 August 2023   by radiologybusiness.com
B. Braun Win Clearance for Continuous Infusion Pump System in MRI Suite
'''''B. Braun Medical announced it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for SpaceStation MRI, a system that improves the use of infusion pumps in the ...'
Sunday, 30 August 2020   by www.diagnosticimaging.com
Canon scores FDA clearance for artificial intelligence engine that bolsters MRI quality
'''''Canon Medical Systems USA has earned 510(K) clearance from the U.S. Food and Drug Administration for a deep learning tool that helps sharpen MR image quality. Following the approval, the ...'
Friday, 20 March 2020   by www.radiologybusiness.com
FDA Approves Motion Correction System for MRI Scanners
'''''KinetiCor, Inc., the only approved manufacturer of optical motion detection solutions for MRI scanners, received 510(k) clearance from the U.S. Food and Drug Administration Wednesday for its ...'
Wednesday, 19 February 2020   by www.diagnosticimaging.com
GE Healthcare announces FDA approval of macrocyclic MRI contrast agent Clariscan
'''''The U.S. Food and Drug Administration (FDA) has approved Clariscan, a macrocyclic, ionic, gadolinium-based, magnetic resonance imaging (MRI) contrast agent, expanding the GE Healthcare portfolio ...'
Monday, 4 November 2019   by www.itnonline.com
FDA Expands Pediatric Age Range for MultiHance Contrast Agent
'''''Bracco Diagnostics announced that the Food and Drug Administration (FDA) has approved an expanded age range for MultiHance (gadobenate dimeglumine) contrast agent to include magnetic ...'
Tuesday, 30 January 2018   by www.empr.com
FDA Drug Safety Communication: FDA warns that gadolinium-based contrast agents (GBCAs) are retained in the body; requires new class warnings
'''''The U.S. Food and Drug Administration (FDA) is requiring a new class warning and other safety measures for all gadolinium-based contrast agents (GBCAs) for magnetic resonance imaging (MRI) ...'
Tuesday, 19 December 2017   by www.fda.gov
Elbit Imaging Ltd. Announces The Taiwanese Food And Drug Administration (TFDA) Approved Insightec's Exablate Neuro For The Treatment Of Esseential Tremor
'''''Elbit Imaging Ltd. (TASE, NASDAQ: EMITF) (Elbit or the Company) announced today, that Insightec Ltd. (Insightec) informed that the Taiwanese Food and Drug Administration (TFDA) has ...'
Friday, 24 November 2017   by www.digitaljournal.com
FDA clears first neonatal magnetic resonance imaging device
'''''Today, the U.S. Food and Drug Administration cleared the first magnetic resonance imaging (MRI) device specifically for neonatal brain and head imaging in neonatal intensive care ...'
Thursday, 20 July 2017   by www.fda.gov
New imaging technique shows effectiveness of cystic fibrosis drug
'''''According to the Cystic Fibrosis Foundation, more than 30,000 Americans are living with the disorder. It currently has no cure, though a drug approved by the Food and Drug Administration treats ...'
Wednesday, 12 April 2017   by www.sciencedaily.com
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- Ross MacDonald
 
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