
Mnlase, Inc.
Free shipping on orders over $99 · 30-day returns
LASER DELIVERY PROBE is an FDA 510(k)-cleared medical device (K944282) manufactured by Mnlase, 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 October 31, 1994. Regulation: 8.