
Intra Lase Corp.
Free shipping on orders over $99 · 30-day returns
IFS LASER SYSTEM is an FDA 510(k)-cleared medical device (K073404) manufactured by Intra Lase 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 April 24, 2008. Regulation: 8.