MANIPULATOR & INJECTOR, UTERINE

MANIPULATOR & INJECTOR, UTERINE is an FDA 510(k)-cleared medical device (K770727) manufactured by National Catheter Co. Div. Mallinckrodt. 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 25, 1977. Regulation: 8.