GeneralDevices & AI clearances

Philips EPIQ Inspira and Affiniti ultrasound cleared by FDA

U.S. FDA1w ago

FDA cleared Philips' EPIQ Inspira and Affiniti diagnostic ultrasound systems via 510(k) pathway (product code IYN).

  • Cleared under the FDA Radiology Devices Panel.
  • Philips Ultrasound, LLC is the applicant.
Read the source

Automated summary

RadPigeon summaries are original and for information only. They are not clinical advice.