FDA 510(k) Application Details - K970600

Device Classification Name	Bandage, Liquid   More FDA Info for this Device
510(K) Number	K970600
Device Name	Bandage, Liquid
Applicant	DERMARX CORP. 400 SOUTH COLORADO BLVD.,#420 DENVER, CO 80222 US Other 510(k) Applications for this Company
Contact	MARYANNE CARROLL 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	02/18/1997
Decision Date	05/08/1997
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review