
Kimberly-Clark Corp.
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KOTEX PROFILE SHAPED MAXI PAD is an FDA 510(k)-cleared medical device (K861902) manufactured by Kimberly-Clark Corp.. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on June 8, 1986. Regulation: 8.

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