REMSTAR WTIH RAMP AND REMOTE MODIFICATION

REMSTAR WTIH RAMP AND REMOTE MODIFICATION is an FDA 510(k)-cleared medical device (K920699) 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 6, 1992. Regulation: 8.