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Vitaid, Ltd.
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PEDIATRIC CUFFED AND UNCUFFED ET TUBES; STANDARD CUFFED AND UNCUFFED ET TUBES is an FDA 510(k)-cleared medical device (K050803) manufactured by Vitaid, 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 June 29, 2005. Regulation: 8.