AUTO SUTURE MODIFIED ENDO STREAM SUC./IRRI. DEVICE

AUTO SUTURE MODIFIED ENDO STREAM SUC./IRRI. DEVICE is an FDA 510(k)-cleared medical device (K905426) manufactured by United States Surgical, A Division of Tyco Healthc. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 10, 1991. Regulation: 8.