GeneralDevices & AI clearances

FDA Clears Philips Alturion Series Diagnostic Ultrasound

U.S. FDA2w ago

FDA cleared the Philips Alturion Series diagnostic ultrasound system through the 510(k) pathway (product code IYN, radiology committee).

  • 510(k) premarket notification submitted by Philips Ultrasound, LLC.
  • Assigned FDA product code IYN under the radiology device committee.
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