MYOSURE HYSTEROSCOPIC TISSUE REMOVAL SYSTEM

MYOSURE HYSTEROSCOPIC TISSUE REMOVAL SYSTEM is an FDA 510(k)-cleared medical device (K100559) manufactured by Interlace Medical, 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 March 29, 2010. Regulation: 8.