ARCADIA MEDICAL SILICONE WIRE REINFORCED ENDOTRACHEAL TUBES

ARCADIA MEDICAL SILICONE WIRE REINFORCED ENDOTRACHEAL TUBES is an FDA 510(k)-cleared medical device (K060094) manufactured by Arcadia Medical Corporation. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 7, 2006. Regulation: 8.