FORCEPS FOR LAPAROSCOPIC SURGERY OB/GYN USE

FORCEPS FOR LAPAROSCOPIC SURGERY OB/GYN USE is an FDA 510(k)-cleared medical device (K925960) manufactured by Zinnanti Surgical Instruments, 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 June 6, 1994. Regulation: 8.