Luxar Corp.
LUXAR ENDOGUIDE CO2 LASER WAVEGUIDE
SKU K884459UPC GEX
In Stock
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IIFDA 510(k) Cleared (K884459)
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Free shipping on orders over $99 · 30-day returns
Luxar Corp.
Free shipping on orders over $99 · 30-day returns
LUXAR ENDOGUIDE CO2 LASER WAVEGUIDE is an FDA 510(k)-cleared medical device (K884459) manufactured by Luxar Corp.. 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 December 18, 1988. Regulation: 8.
