Nitronox Plus 0-70, Nitronox 0-50, Nitronox Plus 50/50

Nitronox Plus 0-70, Nitronox 0-50, Nitronox Plus 50/50 is an FDA 510(k)-cleared medical device (K202480) manufactured by Parker Hannifin. 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 21, 2021. Regulation: 8.