BLEASE FRONTLINE GENIUS RANGE ANAESTHESIA MACHINE

BLEASE FRONTLINE GENIUS RANGE ANAESTHESIA MACHINE is an FDA 510(k)-cleared medical device (K982137) manufactured by Blease Medical Equipment , Ltd.. 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 8, 1999. Regulation: 8.