ALL PUPOSE URETHRAL CATHETER

ALL PUPOSE URETHRAL CATHETER is an FDA 510(k)-cleared medical device (K803080) manufactured by American Hospital Supply 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 December 21, 1980. Regulation: 8.