REMSTAR AFLEX CPAP SYSTEM

REMSTAR AFLEX CPAP SYSTEM is an FDA 510(k)-cleared medical device (K063830) 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 March 8, 2007. Regulation: 8.