Philips secures FDA clearance for Elevate Plus AI ultrasound upgrade

Philips has received 510(k) clearance for Elevate Plus, which adds imaging and AI capabilities to its EPIQ Elite and Affiniti ultrasound systems. With the clearance, Philips brings workflow automation and image quality features to ultrasound, aiming to standardise routine examinations. Elevate Plus is designed to deliver more consistent images at faster speeds across different healthcare staff. Credit: Koninklijke Philips N.V. Philips has received the US Food and Drug Administration (FDA) 510(k) clearance for Elevate Plus, an upgrade that adds new imaging and AI capabilities to its EPIQ Elite and Affiniti ultrasound systems. The company confirmed it has also received the…

Source: Medical Device Network