(SPAG) MODEL SPAG-2 6000 SERIES

(SPAG) MODEL SPAG-2 6000 SERIES is an FDA 510(k)-cleared medical device (K871427) manufactured by Viratek, 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 October 5, 1987. Regulation: 8.