
Respironics, Inc.
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MODIFICATION TO REMSTAR AUTO CPAP SYSTEM is an FDA 510(k)-cleared medical device (K031460) 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 June 23, 2003. Regulation: 8.