MEDLINE RED RUBBER URETHRAL CATHETER

MEDLINE RED RUBBER URETHRAL CATHETER is an FDA 510(k)-cleared medical device (K092250) manufactured by Medline Industries, 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 January 20, 2010. Regulation: 8.