REPROCESSED TROCARS AND CANNULAS

REPROCESSED TROCARS AND CANNULAS is an FDA 510(k)-cleared medical device (K012644) manufactured by Surgical Instruments Service and Savings, 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 28, 2002. Regulation: 8.