KEMI LABS - ADHESIVE BANDAGE REMOVER

KEMI LABS - ADHESIVE BANDAGE REMOVER is an FDA 510(k)-cleared medical device (K895293) manufactured by Kemi Labs, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on February 8, 1990. Regulation: 8.