LUXTRON MODEL 3100/3101/3102 MULTICHANNEL

LUXTRON MODEL 3100/3101/3102 MULTICHANNEL is an FDA 510(k)-cleared medical device (K923189) manufactured by Luxtron. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 27, 1994. Regulation: 8.