FDA 510(k) Application Details - K953751

Device Classification Name	Apparatus, Hemoperfusion, Sorbent   More FDA Info for this Device
510(K) Number	K953751
Device Name	Apparatus, Hemoperfusion, Sorbent
Applicant	HEMOCLEANSE, INC. 2700 KENT AVE. WEST LAFAYETTE, IN 47906 US Other 510(k) Applications for this Company
Contact	STEPHEN R ASH 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	08/10/1995
Decision Date	02/15/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review