ClearanceBrief
Company ยท US

Renal Solutions, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2003 to 2013. Name variants (Inc, Corp, punctuation) are merged.

9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
FKTSystem, Dialysate Delivery, Sorbent Regenerated6
KDIDialyzer, High Permeability With Or Without Sealed Dialysate System3

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Feb 15, 2013K1238352008 HEMODIALYSIS SORBENT SYSTEM
Renal Solutions, Inc.
FKT
Aug 17, 2012K121497VENOFER PUMP
Renal Solutions, Inc.
KDI
Feb 10, 2011K103564VENOFER PUMP
Renal Solutions, Inc.
KDI
Aug 13, 2010K0933622008 HEMODIALYSIS SORBENT SYSTEM
Renal Solutions, Inc.
FKT
Jul 9, 2010K093964VENOFER PUMP
Renal Solutions, Inc.
KDI
May 25, 2007K070739ALLIENT SORBENT HEMODIALYSIS SYSTEM, MODEL# 1500
Renal Solutions, Inc.
FKT
May 24, 2006K060381ALLIENT SORBET HEMODIALYSIS SYSTEM, MODEL 1100
Renal Solutions, Inc.
FKT
Jun 3, 2005K043574ALLIENT SORBENT HEMODIALYSIS SYSTEM, MODEL 1000
Renal Solutions, Inc.
FKT
Sep 17, 2003K031099SORB+HISORB+CARTRIDGE
Renal Solutions, Inc.
FKT

Latest recalls

DateFirm and productCodeLinked 510(k)
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