510(k) K930181

BIOPURE DIALYSATE CONCENTRATE MIX SYST/CONCENTRATE by Fresenius USA, Inc. — Product Code FKP

K930181 is an FDA 510(k) premarket notification submitted by Fresenius USA, Inc. for the device "BIOPURE DIALYSATE CONCENTRATE MIX SYST/CONCENTRATE". The FDA issued a decision of Substantially Equivalent on November 29, 1995. The device falls under product code FKP (System, Dialysate Delivery, Single Patient), a Class II device regulated under 21 CFR 876.5820. Fresenius USA, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 29, 1995
Date Received
January 14, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Dialysate Delivery, Single Patient
Device Class
Class II
Regulation Number
876.5820
Review Panel
GU
Submission Type