K-number	K062602
Device name	BAND-AID(R) BRAND LIQUID BANDAGE
Applicant	Johnson & Johnson Consumer Companies, Inc.
Product code	KMF
Device class	Class I
Decision date	Dec 11, 2006
Decision	Substantially Equivalent
Regulation	880.5090

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View the full FDA submission: accessdata.fda.gov

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BAND-AID(R) BRAND LIQUID BANDAGE

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