ASI UROPLASTY LASER CYSTOSCOPE

ASI UROPLASTY LASER CYSTOSCOPE is an FDA 510(k)-cleared medical device (K921990) manufactured by Advanced Surgical Intervention, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 27, 1992. Regulation: 8.