INTRA-UTERINE TRANSFER, INTRA-FOLOPIAN TRANSFER

INTRA-UTERINE TRANSFER, INTRA-FOLOPIAN TRANSFER is an FDA 510(k)-cleared medical device (K983604) manufactured by Washington Regulatory Services. 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 May 26, 1999. Regulation: 8.