KSEA MODEL 26012CH ELECTRONIC LAPAROFLATOR

KSEA MODEL 26012CH ELECTRONIC LAPAROFLATOR is an FDA 510(k)-cleared medical device (K951961) manufactured by KARL STORZ Endoscopy-America, 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 July 31, 1995. Regulation: 8.