INSTRUMED FORCEPS OBSTETRICAL/GYNAECOLOGICAL

INSTRUMED FORCEPS OBSTETRICAL/GYNAECOLOGICAL is an FDA 510(k)-cleared medical device (K092840) manufactured by Instrumed International, 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 December 2, 2009. Regulation: 8.