SINGLE SITE FLEXIBLE BLADELESS OBTURATOR

SINGLE SITE FLEXIBLE BLADELESS OBTURATOR is an FDA 510(k)-cleared medical device (K101671) 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 June 24, 2010. Regulation: 8.