RUSCH MMG/O'NEIL CATHETER

RUSCH MMG/O'NEIL CATHETER is an FDA 510(k)-cleared medical device (K010420) manufactured by Rusch, 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 May 8, 2001. Regulation: 8.