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Kimberly-Clark Corp.
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KIMBERLY-CLARK GASTROINTESTINAL ANCHOR SET WITH SAF-T-PEXY FASTENERS, ENTERNAL ACCESS DILATION SYSTEM is an FDA 510(k)-cleared medical device (K093312) manufactured by Kimberly-Clark Corp.. 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 December 7, 2009. Regulation: 8.

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