FDA 510(k) Application Details - K062602

Device Classification Name	Bandage, Liquid   More FDA Info for this Device
510(K) Number	K062602
Device Name	Bandage, Liquid
Applicant	JOHNSON & JOHNSON CONSUMER COMPANIES, INC. 199 GRANDVIEW ROAD SKILLMAN, NJ 08558-9498 US Other 510(k) Applications for this Company
Contact	MICHELLE R TURK Other 510(k) Applications for this Contact
Regulation Number	880.5090   More FDA Info for this Regulation Number
Classification Product Code	KMF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/01/2006
Decision Date	12/11/2006
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review