RUSCH ENDOTEST CUFF PRESSURE MONITOR

RUSCH ENDOTEST CUFF PRESSURE MONITOR is an FDA 510(k)-cleared medical device (K951046) manufactured by Rusch Intl.. 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 5, 1995. Regulation: 8.