Luxar Corp.
MODIFIED LUXAR LX-20 FAMILY CO2 LASER SYSTEM
SKU K953074UPC GEX
In Stock
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IIFDA 510(k) Cleared (K953074)
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Free shipping on orders over $99 · 30-day returns
Luxar Corp.
Free shipping on orders over $99 · 30-day returns
MODIFIED LUXAR LX-20 FAMILY CO2 LASER SYSTEM is an FDA 510(k)-cleared medical device (K953074) 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 August 27, 1995. Regulation: 8.
