UROPLASTY RIGID ENDOSCPIC NEEDLES

UROPLASTY RIGID ENDOSCPIC NEEDLES is an FDA 510(k)-cleared medical device (K121337) manufactured by Uroplasty, 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 August 2, 2012. Regulation: 8.