FDA 510(k) Application Details - K033262

Device Classification Name	Apparatus, Hemoperfusion, Sorbent   More FDA Info for this Device
510(K) Number	K033262
Device Name	Apparatus, Hemoperfusion, Sorbent
Applicant	GAMBRO RENAL PRODUCTS 10810 W. COLLINS AVE. LAKEWOOD, CO 80215 US Other 510(k) Applications for this Company
Contact	KAE MILLER Other 510(k) Applications for this Contact
Regulation Number	876.5870   More FDA Info for this Regulation Number
Classification Product Code	FLD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/09/2003
Decision Date	05/27/2005
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