COOPER LASER SONICS ND: YAG LASER, MODEL 8008

COOPER LASER SONICS ND: YAG LASER, MODEL 8008 is an FDA 510(k)-cleared medical device (K853117) 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 August 11, 1986. Regulation: 8.