KSEA SEMM TISSUR PUNCH

KSEA SEMM TISSUR PUNCH is an FDA 510(k)-cleared medical device (K943053) manufactured by Karl Storz Endoskop GmbH. 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 20, 1995. Regulation: 8.