AUTO SUTURE SURGIPORT DEPTH GUIDE AND SKIRT

AUTO SUTURE SURGIPORT DEPTH GUIDE AND SKIRT is an FDA 510(k)-cleared medical device (K893707) manufactured by United States Surgical, A Division of Tyco Healthc. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 14, 1989. Regulation: 8.