KOTEX DISCRETE DIGITAL TAMPONS, REG.,SUPER,SUPER+

KOTEX DISCRETE DIGITAL TAMPONS, REG.,SUPER,SUPER+ is an FDA 510(k)-cleared medical device (K930149) 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 March 1, 1994. Regulation: 8.