
Draeger Medical, Inc.
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FABIUS GS ANESTHESIA SYSTEM, MODEL FABIUS GS is an FDA 510(k)-cleared medical device (K011404) manufactured by Draeger Medical, 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 February 21, 2002. Regulation: 8.