MODEL 4900 ND:YAG LASER FOR GASTRO & GENITOUR APPL

MODEL 4900 ND:YAG LASER FOR GASTRO & GENITOUR APPL is an FDA 510(k)-cleared medical device (K880171) 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 April 10, 1988. Regulation: 8.