DUREX PLAY TEMPTATIONS ASSORTED LUBRICANTS

DUREX PLAY TEMPTATIONS ASSORTED LUBRICANTS is an FDA 510(k)-cleared medical device (K060098) manufactured by Ssl Americas, Inc.. 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 June 7, 2006. Regulation: 8.