ACCU-PULSE 1000 CO2 SURGICAL LASER SYSTEM

ACCU-PULSE 1000 CO2 SURGICAL LASER SYSTEM is an FDA 510(k)-cleared medical device (K983543) manufactured by Argus Photonics Group. 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 December 15, 1998. Regulation: 8.