
Nu Vasive, Incorporated
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NUVASIVE EMG ENDOTRACHEAL TUBE is an FDA 510(k)-cleared medical device (K133530) manufactured by Nu Vasive, Incorporated. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 1, 2014. Regulation: 8.

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