ACCU-PULSE CARBON DIOXIDE LASER SYSTEM

ACCU-PULSE CARBON DIOXIDE LASER SYSTEM is an FDA 510(k)-cleared medical device (K971830) 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 August 13, 1997. Regulation: 8.