
Laser Peripherals, LLC
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BARE LASER FIBER MODELS DBLF-40, DBLF-60, DBLF-60-1, DCLF-600B, DSLF-60, DBLF-100 is an FDA 510(k)-cleared medical device (K030959) 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 April 24, 2003. Regulation: 8.