FDA 510(k) Application Details - K984207

Device Classification Name	Bandage, Liquid   More FDA Info for this Device
510(K) Number	K984207
Device Name	Bandage, Liquid
Applicant	ARGENTUM INTERNATIONAL LLC. PO BOX 429 LAKEMONT, GA 30552 US Other 510(k) Applications for this Company
Contact	A. BART FLICK 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	11/24/1998
Decision Date	03/19/2007
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