FDA 510(k) Application Details - K964016

Device Classification Name	Bandage, Liquid   More FDA Info for this Device
510(K) Number	K964016
Device Name	Bandage, Liquid
Applicant	JOHNSON & JOHNSON MEDICAL, INC. 2500 ARBROOK BLVD. P.O. BOX 90130 ARLINGTON, TX 76004-0130 US Other 510(k) Applications for this Company
Contact	RALPH H LARSEN 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	10/07/1996
Decision Date	12/31/1996
Decision	SN - Substantially Equivalent for Some Indications
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status
Type	Traditional
Reviewed By Third Party	N
Expedited Review