ENDOSCOPIC LASER DELIVERY SYSTEM-LASERTX

ENDOSCOPIC LASER DELIVERY SYSTEM-LASERTX is an FDA 510(k)-cleared medical device (K023257) manufactured by Prosurg, 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 27, 2003. Regulation: 8.