TROCAR SYSTEM ACCORDING TO HASSON

TROCAR SYSTEM ACCORDING TO HASSON is an FDA 510(k)-cleared medical device (K990237) manufactured by Olympus America, 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 11, 1999. Regulation: 8.