TRI-MED 511 INFANT RESPIRATION MONITOR

TRI-MED 511 INFANT RESPIRATION MONITOR is an FDA 510(k)-cleared medical device (K833397) manufactured by Tri-Med, 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 November 27, 1983. Regulation: 8.