Luxar Corp.
LUXAR ENDOGUIDE CO2 LASER WAVEGUIDE (NEURO.)
SKU K897040UPC GEX
In Stock
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IIFDA 510(k) Cleared (K897040)
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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 (NEURO.) is an FDA 510(k)-cleared medical device (K897040) 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 February 12, 1990. Regulation: 8.
