
Computer Motion, Inc.
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HERMES CONTROL CENTER, WITH CONTROL OF THE AESOP 3000HR (HERMES READY). is an FDA 510(k)-cleared medical device (K991444) 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 June 24, 1999. Regulation: 8.