UROMED NEEDLE GRASPER

UROMED NEEDLE GRASPER is an FDA 510(k)-cleared medical device (K974137) manufactured by Uromed Corp.. 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 January 29, 1998. Regulation: 8.