
Luxar Corp.
Free shipping on orders over $99 · 30-day returns
LUXAR MODEL LX-20 MINILASE CO2 LASER is an FDA 510(k)-cleared medical device (K896478) 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 7, 1990. Regulation: 8.