FDA 510(k) Application Details - K031263

Device Classification Name	Bandage, Liquid   More FDA Info for this Device
510(K) Number	K031263
Device Name	Bandage, Liquid
Applicant	3M COMPANY 3M CENTER, BLDG. 275-5W-06 ST. PAUL, MN 55133-3275 US Other 510(k) Applications for this Company
Contact	ANNA E MCRIGHT 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	04/21/2003
Decision Date	10/07/2003
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