REMSTAR AUTO A-FLEX

REMSTAR AUTO A-FLEX is an FDA 510(k)-cleared medical device (K091319) manufactured by Respironics Inc., Sleep & Home Respiratory Group. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 2, 2009. Regulation: 8.