FDA 510(k) Application Details - K982378

Device Classification Name	Dialysate Concentrate For Hemodialysis (Liquid Or Powder)   More FDA Info for this Device
510(K) Number	K982378
Device Name	Dialysate Concentrate For Hemodialysis (Liquid Or Powder)
Applicant	SOLUTION TECHNOLOGIES 4825 SOUTH 850 EAST SOUTH OGDEN, UT 84403 US Other 510(k) Applications for this Company
Contact	WILLIAM J GRISWOLD, JR Other 510(k) Applications for this Contact
Regulation Number	876.5820   More FDA Info for this Regulation Number
Classification Product Code	KPO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/08/1998
Decision Date	08/26/1998
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