FDA 510(k) Application Details - K973283

Device Classification Name	Bandage, Liquid   More FDA Info for this Device
510(K) Number	K973283
Device Name	Bandage, Liquid
Applicant	INNOVATIVE TECHNOLOGIES LTD. ROAD THREE, WINSFORD INDUSTRIAL ESTATE WINSFORD, CHESHIRE CW7 3PD GB Other 510(k) Applications for this Company
Contact	PRISCILLA WHITEHEAD COX 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	09/02/1997
Decision Date	10/21/1997
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