COOPERSURGICAL INTRAUTERINE INSEMINATION CATHETER

COOPERSURGICAL INTRAUTERINE INSEMINATION CATHETER is an FDA 510(k)-cleared medical device (K023383) manufactured by Cooper Surgical. 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.