MICROTRAPPER/MICRODIGITRAPPER, MODIFICATION

MICROTRAPPER/MICRODIGITRAPPER, MODIFICATION is an FDA 510(k)-cleared medical device (K905520) manufactured by Synectics-Dantec. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 25, 1991. Regulation: 8.