TUCKER EMBRYO CATHETER

TUCKER EMBRYO CATHETER is an FDA 510(k)-cleared medical device (K023017) manufactured by Fertility Technology Resources, 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 December 12, 2002. Regulation: 8.