
Cooper Lasersonics, Inc.
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#6000 ND:YAG LASER SYSTEM UROLOGY/GASTROINTESTINAL is an FDA 510(k)-cleared medical device (K861903) 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 June 19, 1986. Regulation: 8.