DUREX REALFEEL PLEASURE GEL PERSONAL LUBRICANT

DUREX REALFEEL PLEASURE GEL PERSONAL LUBRICANT is an FDA 510(k)-cleared medical device (K131643) manufactured by Reckitt Benckiser, LLC. 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 December 16, 2014. Regulation: 8.