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# FDA Clears Phillips New MR System
- URL: https://www.fdaweb.com/fda-clears-phillips-new-mr-system/
- Published: 2018-06-05T12:00:00.000Z
- Updated: 2026-09-15T00:10:21.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5141607

FDA has cleared a Royal Philips 510(k) for the Ingenia Elition 3.0T magnetic resonance (MR) device and two clinical applications, Philips Compressed SENSE and 3D APT. The device and apps provide faster exam times and improved analytics to allow automatic planning, scanning and exam processing, the company says. [3D APT](https://www.usa.philips.com/healthcare/product/HCNMRF201/3d-apt-mr-clinical-applications?ref=fdaweb.com) is described as a contrast-free brain MR imaging solution that addresses the need for more confident diagnosis in neuro oncology. “By differentiating low-grade and high-grade gliomas, radiologists have the ability to better understand a tumor's progression and determine the effect of treatment,” Royal Philips says.