ACCU-BEAM LASER BLOCK 301513BG385/BEAM SPLITTERS 301513BG39

ACCU-BEAM LASER BLOCK 301513BG385/BEAM SPLITTERS 301513BG39 is an FDA 510(k)-cleared medical device (K963193) manufactured by Transamerican Technologies Intl.. 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 12, 1996. Regulation: 8.