
Chilecom Medical Devices Co., Ltd.
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ENDOTRACHEAL TUBE is an FDA 510(k)-cleared medical device (K080105) manufactured by Chilecom Medical Devices Co., Ltd.. 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 12, 2009. Regulation: 8.