MORTON IUI CATHETERS

MORTON IUI CATHETERS is an FDA 510(k)-cleared medical device (K041470) 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 November 21, 2004. Regulation: 8.