ENDOSCOPIC HYSTERECTOMY AND UTERUS MANIPULATOR

ENDOSCOPIC HYSTERECTOMY AND UTERUS MANIPULATOR is an FDA 510(k)-cleared medical device (K964276) manufactured by Richard Wolf Medical Instruments Corp.. 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 November 24, 1997. Regulation: 8.