
Pfizer Laser Systems
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35 WATT SURGICAL CARBON DIOXIDE LASER SYSTEM is an FDA 510(k)-cleared medical device (K896049) 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 January 10, 1990. Regulation: 8.