GE HealthCare Says FDA Clears Updated Ultrasound Devices

MT Newswires Live
28 Jan

GE HealthCare Technologies (GEHC) said Tuesday it has received 510(k) clearance from the US Food and Drug Administration for its updated portfolio of Voluson Expert Series ultrasound systems.

The company said the Voluson Expert 22, 20, and 18 systems integrate artificial intelligence tools to enhance imaging quality and streamline workflows.

GE Healthcare said it plans to showcase the systems at the Society for Maternal-Fetal Medicine meeting in Denver.

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