CODMAN NEUROLASE LASER SYSTEM/MODIFICATION

CODMAN NEUROLASE LASER SYSTEM/MODIFICATION is an FDA 510(k)-cleared medical device (K905511) manufactured by I.L. Med, 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 4, 1991. Regulation: 8.