DEVILBISS OXYGEN ENRICHER

DEVILBISS OXYGEN ENRICHER is an FDA 510(k)-cleared medical device (K770157) manufactured by The Devilbiss Co.. 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 6, 1977. Regulation: 8.