FDA 510(k) Application Details - K961706

Device Classification Name	Separator, Automated, Blood Cell And Plasma, Therapeutic   More FDA Info for this Device
510(K) Number	K961706
Device Name	Separator, Automated, Blood Cell And Plasma, Therapeutic
Applicant	FRESENIUS USA, INC. 2637 SHADELANDS DR. WALNUT CREEK, CA 94598 US Other 510(k) Applications for this Company
Contact	TOM FOLDEN Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	LKN Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/02/1996
Decision Date	07/31/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	-
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review