AMI REPROCESSED MULTIPLE CLIP APPLIERS

AMI REPROCESSED MULTIPLE CLIP APPLIERS is an FDA 510(k)-cleared medical device (K032980) manufactured by Vanguard Medical Concepts, 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 December 17, 2003. Regulation: 8.