FOCUS TOUCH CONCEPTION SYSTEM

FOCUS TOUCH CONCEPTION SYSTEM is an FDA 510(k)-cleared medical device (K112200) manufactured by Intimate Bridge 2 Conception, 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 September 5, 2012. Regulation: 8.