SINGLE USE MANUAL RESUSCITATOR PEEP VALVE

SINGLE USE MANUAL RESUSCITATOR PEEP VALVE is an FDA 510(k)-cleared medical device (K932799) manufactured by Engineered Medical Systems. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 2, 1993. Regulation: 8.