MODIFICATION TO: GIRAFFE AND PANDA WARMER

MODIFICATION TO: GIRAFFE AND PANDA WARMER is an FDA 510(k)-cleared medical device (K090697) manufactured by Ohmeda Medical. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 15, 2009. Regulation: 8.