MODIFICATION TO HERMES OPERATING ROOM CONTROL CENTER

MODIFICATION TO HERMES OPERATING ROOM CONTROL CENTER is an FDA 510(k)-cleared medical device (K022897) manufactured by Computer Motion, Inc.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 10, 2002. Regulation: 8.