
Eltech S.R.L
Free shipping on orders over $99 · 30-day returns
K-LASER K-1200, MODEL 12 W is an FDA 510(k)-cleared medical device (K091497) manufactured by Eltech S.R.L. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 18, 2009. Regulation: 8.