
Pfizer Laser Systems
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MODEL 20-CH CARBON DIOXIDE LASER W/ADD'L USES is an FDA 510(k)-cleared medical device (K900253) manufactured by Pfizer Laser Systems. 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 April 4, 1990. Regulation: 8.