ERBIUM 2000 LASER FAMILY

ERBIUM 2000 LASER FAMILY is an FDA 510(k)-cleared medical device (K972915) manufactured by Phantom Technologies, 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 December 18, 1997. Regulation: 8.