RESPIRONICS SLEEPEASY NASAL CPAP SYS

RESPIRONICS SLEEPEASY NASAL CPAP SYS is an FDA 510(k)-cleared medical device (K843889) manufactured by Respironics, 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 December 3, 1984. Regulation: 8.