KELOCOTE SCAR GEL AND KELOCOTE LASER GEL

KELOCOTE SCAR GEL AND KELOCOTE LASER GEL is an FDA 510(k)-cleared medical device (K973572) manufactured by Hanson Medical, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on October 20, 1997. Regulation: 8.