FDA 510(k) Application Details - K970153

Device Classification Name	Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic   More FDA Info for this Device
510(K) Number	K970153
Device Name	Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic
Applicant	PROCYTE CORP. 12040 115TH AVE. N.E., #210 KIRKLAND, WA 98034 US Other 510(k) Applications for this Company
Contact	PAUL KETTERIDGE Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	MGQ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/16/1997
Decision Date	06/05/1997
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	-
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review