
Core Dynamics, Inc.
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LAPAROSCOPIC TROCAR OBTURATOR, 5MM, 10/11MM, 10/12MM is an FDA 510(k)-cleared medical device (K953903) manufactured by Core Dynamics, 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 October 19, 1995. Regulation: 8.