CAP-ONE, MODEL TG-920P

CAP-ONE, MODEL TG-920P is an FDA 510(k)-cleared medical device (K040875) manufactured by Nihon Kohden America, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 14, 2004. Regulation: 8.