FORGARTY CHIN PERIPHERAL INTRAOPERATIVE

FORGARTY CHIN PERIPHERAL INTRAOPERATIVE is an FDA 510(k)-cleared medical device (K830733) manufactured by American Edwards Laboratories. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 17, 1983. Regulation: 8.