DATEX-OHMEDA ANESTHESIA VAPORIZER, MODEL D-TEC

DATEX-OHMEDA ANESTHESIA VAPORIZER, MODEL D-TEC is an FDA 510(k)-cleared medical device (K990132) manufactured by Datex-Ohmeda, 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 January 20, 1999. Regulation: 8.