MODEL 1712 CATHETER WITHDRAWAL SYS FOR URETHRAL PR

MODEL 1712 CATHETER WITHDRAWAL SYS FOR URETHRAL PR is an FDA 510(k)-cleared medical device (K850601) manufactured by Life-Tech Intl., 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 April 24, 1985. Regulation: 8.