FDA 510(k) Application Details - K992032

Device Classification Name	Bandage, Liquid   More FDA Info for this Device
510(K) Number	K992032
Device Name	Bandage, Liquid
Applicant	ACRYMED, INC. 12232 S.W. GARDEN PL. PORTLAND, OR 97223 US Other 510(k) Applications for this Company
Contact	BRUCE GIBBINS 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	06/16/1999
Decision Date	08/19/1999
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