FDA 510(k) Application Details - K972329

Device Classification Name	Bandage, Liquid   More FDA Info for this Device
510(K) Number	K972329
Device Name	Bandage, Liquid
Applicant	PROCYTE CORP. 8511 154TH AVE., N.E., BLDG. A REDMOND, WA 98052 US Other 510(k) Applications for this Company
Contact	PAUL KETTERIDGE 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	06/23/1997
Decision Date	12/10/1997
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