DUAL LUMEN TRANSCERIVICAL INTRAUTERINE KIT

DUAL LUMEN TRANSCERIVICAL INTRAUTERINE KIT is an FDA 510(k)-cleared medical device (K920044) manufactured by Telos Medical Corp.. 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 2, 1992. Regulation: 8.