ACTOVOX DUO2 OXYGEN CONCENTRATOR SYSTEM

ACTOVOX DUO2 OXYGEN CONCENTRATOR SYSTEM is an FDA 510(k)-cleared medical device (K132205) manufactured by Inova Labs, 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 June 5, 2014. Regulation: 8.