SPAG-2 AEROSOL GENERATOR W/USE OF VIRAZOLE

SPAG-2 AEROSOL GENERATOR W/USE OF VIRAZOLE is an FDA 510(k)-cleared medical device (K870051) 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.