FDA 510(k) Application Details - K991729

Device Classification Name	Bandage, Liquid   More FDA Info for this Device
510(K) Number	K991729
Device Name	Bandage, Liquid
Applicant	FERRIS MFG. CORP. 16 WEST 300 83RD ST. BURR RIDGE, IL 60527 US Other 510(k) Applications for this Company
Contact	THEODORE THORSEN 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	05/20/1999
Decision Date	08/27/1999
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