
Kimberly-Clark Corp.
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KOTEX LIGHTDAYS DEODORANT PANTILINERS is an FDA 510(k)-cleared medical device (K802277) manufactured by Kimberly-Clark Corp.. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 9, 1980. Regulation: 8.

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