FDA 510(k) Application Details - K955453

Device Classification Name	Bandage, Liquid   More FDA Info for this Device
510(K) Number	K955453
Device Name	Bandage, Liquid
Applicant	WESTAIM TECHNOLOGIES, INC. 555 13TH STREET, N.W. WASHINGTON, DC 20004-1109 US Other 510(k) Applications for this Company
Contact	JONATHAN S KAHAN 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	11/29/1995
Decision Date	05/31/1996
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