510(k) K062602

BAND-AID(R) BRAND LIQUID BANDAGE by Johnson & Johnson Consumer Companies, Inc. — Product Code KMF

K062602 is an FDA 510(k) premarket notification submitted by Johnson & Johnson Consumer Companies, Inc. for the device "BAND-AID(R) BRAND LIQUID BANDAGE". The FDA issued a decision of Substantially Equivalent on December 11, 2006. The device falls under product code KMF (Bandage, Liquid), a Class I device regulated under 21 CFR 880.5090. Johnson & Johnson Consumer Companies, Inc. has at least 1 other 510(k) clearance on record.