K-Y BRAND LIQUIBEADS

K-Y BRAND LIQUIBEADS is an FDA 510(k)-cleared medical device (K122061) manufactured by Johnson & Johnson Healthcare Products. 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 November 7, 2013. Regulation: 8.