KSEA CHARDONNES MORCELLATION KNIFE

KSEA CHARDONNES MORCELLATION KNIFE is an FDA 510(k)-cleared medical device (K000212) manufactured by KARL STORZ Endoscopy-America, Inc.. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 20, 2000. Regulation: 8.