MODEL 8900 ND:YAG LASER

MODEL 8900 ND:YAG LASER is an FDA 510(k)-cleared medical device (K863433) manufactured by Cooper Lasersonics, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 16, 1986. Regulation: 8.