FDA 510(k) Application Details - K091360

Device Classification Name	Dialyzer Reprocessing System   More FDA Info for this Device
510(K) Number	K091360
Device Name	Dialyzer Reprocessing System
Applicant	NOVAFLUX TECHNOLOGIES 1 WALL STREET PRINCETON, NJ 08540 US Other 510(k) Applications for this Company
Contact	MOHAMED E LABIB Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	LIF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/08/2009
Decision Date	11/03/2010
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review