FLYNN SERIES III BAG/MASK UNIT-

FLYNN SERIES III BAG/MASK UNIT- is an FDA 510(k)-cleared medical device (K832495) manufactured by O-Two Systems Intl., 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 September 28, 1983. Regulation: 8.