CATHETERIZATION PROCED. TRAY, URETHRAL

CATHETERIZATION PROCED. TRAY, URETHRAL is an FDA 510(k)-cleared medical device (K780124) manufactured by Walpak Co.. 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 February 20, 1978. Regulation: 8.