
Laser Peripherals, LLC
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LASEGUIDE CAT # CLF-600D & CLF-1000D is an FDA 510(k)-cleared medical device (K901786) manufactured by Laser Peripherals, 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 June 26, 1990. Regulation: 8.