KSEA SAWAHLE ELECTROMECHANICAL MORCELLATOR

KSEA SAWAHLE ELECTROMECHANICAL MORCELLATOR is an FDA 510(k)-cleared medical device (K011841) manufactured by Karl Storz Endoscopy. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 9, 2001. Regulation: 8.