
Mnlase, Inc.
Free shipping on orders over $99 · 30-day returns
MODEL 230-SAC LASER DELIVERY PROBE is an FDA 510(k)-cleared medical device (K944629) 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 November 2, 1994. Regulation: 8.