MINIOX 3000 OXYGEN MONITOR

MINIOX 3000 OXYGEN MONITOR is an FDA 510(k)-cleared medical device (K961644) manufactured by Minesafety Appliances Co.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 24, 1996. Regulation: 8.