
The Laryngeal Mask Co., Ltd.
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ILM ENDOTRACHEAL TUBE is an FDA 510(k)-cleared medical device (K991580) manufactured by The Laryngeal Mask 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 3, 2000. Regulation: 8.

ADC
SKU DX606933

MDF
SKU DX683863

3M Littmann
SKU DX771242

Welch Allyn
SKU DX297280