WECK REUSABLE OBTURATOR

WECK REUSABLE OBTURATOR is an FDA 510(k)-cleared medical device (K121796) manufactured by Teleflexmedical, 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 10, 2012. Regulation: 8.