KNOT PUSHER, SPOON FORCEPS AND BIOPSY FORCEPS

KNOT PUSHER, SPOON FORCEPS AND BIOPSY FORCEPS is an FDA 510(k)-cleared medical device (K940049) manufactured by Baxter Healthcare Corp. 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 5, 1994. Regulation: 8.