CODMAN LASER BACKSTOP

CODMAN LASER BACKSTOP is an FDA 510(k)-cleared medical device (K853626) manufactured by Codman & Shurtleff, 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 February 6, 1986. Regulation: 8.