POISE PERSONAL LUBRICANT

POISE PERSONAL LUBRICANT is an FDA 510(k)-cleared medical device (K120650) manufactured by Kimberly-Clark Corporation. 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 July 10, 2012. Regulation: 8.