GE HealthCare Secures FDA Approval for Pediatric Use of Optison Ultrasound Enhancing Agent

Reuters
13 May
GE HealthCare Secures FDA Approval for Pediatric Use of Optison Ultrasound Enhancing Agent

GE HealthCare Technologies Inc. has announced that the U.S. Food and Drug Administration (FDA) has granted a new pediatric indication for their Optison™ ultrasound enhancing agent. This approval is significant as it will enhance the clarity and diagnostic accuracy of echocardiograms for pediatric patients. The Optison agent, notable for being the only polyethylene glycol $(PEG)$-free ultrasound enhancing agent in the U.S., will aid cardiologists in obtaining clearer images to better diagnose heart conditions in children, providing a more comprehensive assessment of ventricular function and potential heart abnormalities or diseases.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. GE HealthCare Technologies Inc. published the original content used to generate this news brief via Business Wire (Ref. ID: 20250513473916) on May 13, 2025, and is solely responsible for the information contained therein.

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