SPUR ADULT WITH OPEN RESERVOIR SYSTEM

SPUR ADULT WITH OPEN RESERVOIR SYSTEM is an FDA 510(k)-cleared medical device (K922707) manufactured by Ambu, 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 18, 1992. Regulation: 8.