CUFF-MATE 2 ENDOTRACHEAL CUFF INFLATOR & MONITOR

CUFF-MATE 2 ENDOTRACHEAL CUFF INFLATOR & MONITOR is an FDA 510(k)-cleared medical device (K902114) manufactured by Diemolding Corp.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 17, 1990. Regulation: 8.