FDS INTIMATE AND INTIMATE WARMING LUBRICANT

FDS INTIMATE AND INTIMATE WARMING LUBRICANT is an FDA 510(k)-cleared medical device (K060145) manufactured by Alberto-Culver USA, 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 April 13, 2006. Regulation: 8.