FDAnews
www.fdanews.com/articles/134551-mindray-device-receives-510-k-clearance

Mindray Device Receives 510(k) Clearance

February 24, 2011
Mindray Medical International Ltd. today announced it has received 510(k) clearance from the FDA for its A5 Anesthesia System. The A5’s user interface is designed to simplify carer usage, allowing more time to be devoted to patient care.