ENDO-LASE CD40 CO2 FOR GYNECOLOGY

ENDO-LASE CD40 CO2 FOR GYNECOLOGY is an FDA 510(k)-cleared medical device (K853903) manufactured by Endo Lase, 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 February 20, 1986. Regulation: 8.