COHERENT ULTRAPULSE S SERIES CO2 SURGICAL LASERS MODEL C AND L

COHERENT ULTRAPULSE S SERIES CO2 SURGICAL LASERS MODEL C AND L is an FDA 510(k)-cleared medical device (K974789) manufactured by Lumenis, 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 March 8, 1998. Regulation: 8.