FDA 510(k) Application Details - K061837

Device Classification Name	Dialyzer, High Permeability With Or Without Sealed Dialysate System   More FDA Info for this Device
510(K) Number	K061837
Device Name	Dialyzer, High Permeability With Or Without Sealed Dialysate System
Applicant	NXSTAGE MEDICAL, INC. 439 SOUTH UNION ST., 5TH FLOOR LAWRENCE, MA 01843 US Other 510(k) Applications for this Company
Contact	NORMA LEMAY 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	06/29/2006
Decision Date	07/31/2006
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