ViewRay Receives FDA 510(k) Clearance for MRI-Guided Radiation Therapy System

  • Small
  • Medium
  • Large

ViewRay has announced it has received FDA 510(k) clearance for its MRI-guided radiation therapy system, according to a news release.


Features of the ViewRay system, which is designed for the treatment of cancer, include continuous soft-tissue imaging and the combination of radiotherapy delivery and simultaneous magnetic resonance imaging.


"FDA clearance of our integrated system is a major milestone in the development of our technology," said ViewRay President and CEO Gregory M. Ayers, MD, PhD, in the release. "It has already been an exciting year for ViewRay, with an additional round of funding and the installation of our first research systems at major U.S. medical centers. Early clinical imaging studies have verified the quality of the system's MR images, and now we're looking forward to clinical applications."


ViewRay is headquartered in Oakwood Village, Ohio.


Related Articles on FDA Clearances:

ETView Medical Receives FDA 510(k) Clearance for Line of Innovative Airway Devices

Medspira Receives FDA 510(k) Clearance for Anorectal Manometry Device

MAQUET Cardiovascular Receives FDA 510(k) Clearance for New Intra-Aortic Balloon Catheter Sizes

Copyright © 2021 Becker's Healthcare. All Rights Reserved. Privacy Policy. Cookie Policy. Linking and Reprinting Policy.


Featured Webinars

Featured Whitepapers