CATHETERIZATION TRAYS FOLEY AND URETHRAL

CATHETERIZATION TRAYS FOLEY AND URETHRAL is an FDA 510(k)-cleared medical device (K791427) manufactured by Intermed, 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 September 6, 1979. Regulation: 8.