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MRI News Service:
'Food and Drug Administration' |
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| Result: Searchterm 'Food and Drug Administration' found in 73 news | | Result Pages | | More Results:  Database (9) |
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 | | | '''''Abbott announced that the US Food and Drug Administration (FDA) has approved expanded MRI labelling for its dorsal root ganglion (DRG) stimulation therapy, the Proclaim DRG neurostimulation ...' | | Friday, 19 January 2024 by www.pharmabiz.com |
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| | | '''''The Food and Drug Administration (FDA) has granted 510(k) clearance for a 3T magnetic resonance imaging (MRI)-compatible Small Body Array, which emphasizes a body contouring design and coils that ...' | | | Monday, 15 January 2024 by www.diagnosticimaging.com | |
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| | | '''''he US Food and Drug Administration (FDA) has cleared NM-101 (Terran Biosciences), a cloud-based software platform to analyze neuromelanin-sensitive MRI scans, which could aid in the diagnosis ...' | | | Tuesday, 9 January 2024 by www.medscape.com | |
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| | | '''''Terran Biosciences, Inc., a biotech platform company developing therapeutics and technologies for patients with neuropsychiatric illnesses, has received U.S. Food and Drug Administration ...' | | | Wednesday, 20 December 2023 by www.itnonline.com | |
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| | | ''''' According to the U.S. Food and Drug Administration (FDA), Philips North America LLC is recalling Panorama 1.0T HFO, a magnetic resonance imaging (MRI) system, due to a risk of explosion during ...' | | | Wednesday, 20 December 2023 by www.itnonline.com | |
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| | | '''''A medical equipment manufacturer is investigating after a patient was shot by her own gun triggered by an MRI machine, according to a Food and Drug Administration report. GE Medical Systems ...' | | | Thursday, 14 December 2023 by www.thestar.com.my | |
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| | | '''''The Food and Drug Administration (FDA) has granted 510(k) clearance for BrainSpec Core™, a magnetic resonance spectroscopy (MRS) software that utilizes a reference base of brain chemistry to ...' | | | Tuesday, 28 November 2023 by www.diagnosticimaging.com | |
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| | | '''''The Food and Drug Administration (FDA) has approved a 510(k) conditional clearance for whole-body magnetic resonance imaging (MRI) use in heart failure patients receiving proprietary ...' | | | Monday, 30 October 2023 by www.diagnosticimaging.com | |
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| | | '''''The Food and Drug Administration (FDA) has granted 510(k) clearance for the IGAR system, a robotic guidance and placement system that is compatible with magnetic resonance imaging (MRI). ...' | | | Thursday, 14 September 2023 by www.diagnosticimaging.com | |
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| | | '''''The U.S. Food and Drug Administration (FDA) has announced that Abbott is recalling some of its Proclaim and Infinity neurostimulation systems due to an ongoing issue with patients being unable ...' | | | Thursday, 14 September 2023 by healthimaging.com | |
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