LUCENTLITE, MODEL IMD 010

LUCENTLITE, MODEL IMD 010 is an FDA 510(k)-cleared medical device (K033072) manufactured by Industrial & Medical Design, 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 31, 2004. Regulation: 8.