OCCLUSION CLAMP** DEVICE

OCCLUSION CLAMP** DEVICE is an FDA 510(k)-cleared medical device (K964251) 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 May 22, 1997. Regulation: 8.