CATHETER, NATURAL LATEX URETHRAL

CATHETER, NATURAL LATEX URETHRAL is an FDA 510(k)-cleared medical device (K760440) manufactured by Akron Catheter, 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 October 19, 1976. Regulation: 8.