General Project S.R.L.
AXIOM PULSED LIGHT SYSTEM
SKU K062312UPC GEX
In Stock
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IIFDA 510(k) Cleared (K062312)
1
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General Project S.R.L.
Free shipping on orders over $99 · 30-day returns
AXIOM PULSED LIGHT SYSTEM is an FDA 510(k)-cleared medical device (K062312) manufactured by General Project S.R.L.. 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 October 15, 2006. Regulation: 8.
