GeneralDevices & AI clearances

FDA clears GE Venue Go ultrasound platform

U.S. FDA1w ago

FDA cleared GE's Venue Go ultrasound system via the 510(k) pathway; listed as a radiology ultrasound device under product code IYN.

  • Clearance record filed under FDA Radiology committee.
  • Applicant: GE Medical Systems Ultrasound and Primary care Diagnostics, LLC.
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