ZEPPELIN FORCEPS

ZEPPELIN FORCEPS is an FDA 510(k)-cleared medical device (K891047) 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 March 16, 1989. Regulation: 8.