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Covidien Lp, Formerly Registered AS Kendall
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DOBBHOFF DUAL PORT FEEDING TUBE is an FDA 510(k)-cleared medical device (K112511) manufactured by Covidien Lp, Formerly Registered AS Kendall. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 10, 2012. Regulation: 8.

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