
M.I.S. Technology, Inc.
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M.I.S. TROCAR-CANNULA is an FDA 510(k)-cleared medical device (K925276) manufactured by M.I.S. Technology, 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 May 23, 1993. Regulation: 8.