50W CERALAS D 1950NM DIODE LASER

50W CERALAS D 1950NM DIODE LASER is an FDA 510(k)-cleared medical device (K072682) manufactured by Biolitec, 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 April 17, 2008. Regulation: 8.