SULLIVAN III NASAL CPAP SYSTEM

SULLIVAN III NASAL CPAP SYSTEM is an FDA 510(k)-cleared medical device (K930656) manufactured by Rescare , 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 March 14, 1994. Regulation: 8.