SULLIVAN VPAP II ST-A NASAL VPAP SYSTEM

SULLIVAN VPAP II ST-A NASAL VPAP SYSTEM is an FDA 510(k)-cleared medical device (K974417) manufactured by Resmed Corp. 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, 1998. Regulation: 8.