
Sandstone Medical Technologies, LLC
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LS-40 CO2 LASER SYSTEM MODEL LS-40 is an FDA 510(k)-cleared medical device (K093793) manufactured by Sandstone Medical Technologies, LLC. 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 February 17, 2010. Regulation: 8.