Renal Solutions, Inc.
FDA 510(k) & PMA Approved Devices — 9 products
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Total Devices9
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K123835 | 2008 HEMODIALYSIS SORBENT SYSTEM | FKT | 2013-02-15 | View |
| 510(k) | K121497 | VENOFER PUMP | KDI | 2012-08-17 | View |
| 510(k) | K103564 | VENOFER PUMP | KDI | 2011-02-10 | View |
| 510(k) | K093362 | 2008 HEMODIALYSIS SORBENT SYSTEM | FKT | 2010-08-13 | View |
| 510(k) | K093964 | VENOFER PUMP | KDI | 2010-07-09 | View |
| 510(k) | K070739 | ALLIENT SORBENT HEMODIALYSIS SYSTEM, MODEL# 1500 | FKT | 2007-05-25 | View |
| 510(k) | K060381 | ALLIENT SORBET HEMODIALYSIS SYSTEM, MODEL 1100 | FKT | 2006-05-24 | View |
| 510(k) | K043574 | ALLIENT SORBENT HEMODIALYSIS SYSTEM, MODEL 1000 | FKT | 2005-06-03 | View |
| 510(k) | K031099 | SORB+HISORB+CARTRIDGE | FKT | 2003-09-17 | View |
No matching devices.
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