CARBON DIOXIDE LASER ML 825

CARBON DIOXIDE LASER ML 825 is an FDA 510(k)-cleared medical device (K833528) manufactured by Merrimack Laboratories. 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 18, 1985. Regulation: 8.