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  2. US FDA classifies Philips' recall of imaging machines ... - AOL

    www.aol.com/news/us-fda-classifies-philips...

    (Reuters) -The U.S. FDA said on Thursday it has classified a recall of Philips' medical imaging machines as most serious due to the risk of a detector in some devices unexpectedly falling on ...

  3. US FDA identifies recall of Philips medical imaging devices ...

    www.aol.com/news/us-fda-identifies-recall...

    Philips was recalling some models of the Panorama 1.0T HFO device in the U.S. due to risk of explosion during a "quench procedure" caused by excessive buildup of helium gas. During the procedure ...

  4. Philips shares surge on US recall settlement news - AOL

    www.aol.com/news/philips-pays-1-1-billion...

    April 29, 2024 at 2:11 PM. By Bart H. Meijer. AMSTERDAM (Reuters) -Philips shares surged 35% early on Monday as the medical devices maker announced a smaller-than-expected settlement to resolve ...

  5. Fast low angle shot magnetic resonance imaging - Wikipedia

    en.wikipedia.org/wiki/Fast_low_angle_shot...

    It is the generic form of steady-state free precession imaging. Different manufacturers of MRI equipment use different names for this experiment. Siemens uses the name FLASH, General Electric used the name SPGR (Spoiled Gradient Echo), and Philips uses the name CE-FFE-T1 (Contrast-Enhanced Fast Field Echo) or T1-FFE.

  6. Gradient echo - Wikipedia

    en.wikipedia.org/wiki/Gradient_echo

    Gradient echo is a magnetic resonance imaging (MRI) sequence that has wide variety of applications, from magnetic resonance angiography to perfusion MRI and diffusion MRI. Rapid imaging acquisition allows it to be applied to 2D and 3D MRI imaging. Gradient echo uses magnetic gradients to generate a signal, instead of using 180 degrees ...

  7. FDA warning letter - Wikipedia

    en.wikipedia.org/wiki/FDA_Warning_Letter

    An FDA warning letter is an official message from the United States Food and Drug Administration (FDA) to a manufacturer or other organization that has violated some rule in a federally regulated activity. ... a correspondence that notifies regulated industry about violations that FDA has documented during its inspections or investigations.

  8. History of magnetic resonance imaging - Wikipedia

    en.wikipedia.org/wiki/History_of_magnetic...

    The history of magnetic resonance imaging (MRI) includes the work of many researchers who contributed to the discovery of nuclear magnetic resonance (NMR) and described the underlying physics of magnetic resonance imaging, starting early in the twentieth century. One researcher was American physicist Isidor Isaac Rabi who won the Nobel Prize in ...

  9. Philips cites health risks in recall of ventilators and sleep ...

    www.aol.com/philips-cites-health-risks-recall...

    The medical technology and equipment giant Philips has recalled some of its ventilators and CPAP machines due to a form piece that could potentially become toxic and cause cancer in its users.