FDA 510(k) Application Details - K062922

Device Classification Name	Dialyzer, High Permeability With Or Without Sealed Dialysate System   More FDA Info for this Device
510(K) Number	K062922
Device Name	Dialyzer, High Permeability With Or Without Sealed Dialysate System
Applicant	CHF SOLUTIONS, INC. 7601 NORTHLAND DR. STE. 170 BROOKLYN PARK, MN 55428 US Other 510(k) Applications for this Company
Contact	CHRIS SCAVOTTO Other 510(k) Applications for this Contact
Regulation Number	876.5860   More FDA Info for this Regulation Number
Classification Product Code	KDI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/28/2006
Decision Date	12/13/2006
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review