MODIFICATION TO HERMES O.R. CONTROL CENTER

MODIFICATION TO HERMES O.R. CONTROL CENTER is an FDA 510(k)-cleared medical device (K031720) 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 July 10, 2003. Regulation: 8.