FDA 510(k) Application Details - K002129

Device Classification Name	Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic   More FDA Info for this Device
510(K) Number	K002129
Device Name	Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic
Applicant	FERRIS MFG. CORP. 16 W. 300 83RD ST. BURR RIDGE, IL 60521 US Other 510(k) Applications for this Company
Contact	THEODORE THORSEN 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	07/14/2000
Decision Date	08/25/2000
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	-
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review