K-Y BRAND SENSUAL MIST

K-Y BRAND SENSUAL MIST is an FDA 510(k)-cleared medical device (K053397) manufactured by Mcneil-Ppc, 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 February 16, 2006. Regulation: 8.