FU HONG INDUSTRIES LIMITED SOOTHER TEETHER

FU HONG INDUSTRIES LIMITED SOOTHER TEETHER is an FDA 510(k)-cleared medical device (K093370) manufactured by Fu Hong Industries , Ltd.. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 20, 2010. Regulation: 8.