
Lasermatic, Inc.
Free shipping on orders over $99 · 30-day returns
MODEL 5050 SURGILASER FOR UROLOGY USE is an FDA 510(k)-cleared medical device (K871932) manufactured by Lasermatic, Inc.. 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 March 24, 1988. Regulation: 8.