VPAP III ST-A/KIDSTA MASK SYSTEM

VPAP III ST-A/KIDSTA MASK SYSTEM is an FDA 510(k)-cleared medical device (K060105) manufactured by Resmed, Ltd.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 6, 2006. Regulation: 8.