Rockwell Medical Technologies, Inc.
FDA 510(k) & PMA Approved Devices — 5 products
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Total Devices5
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K062399 | ROCKWELL MEDICALTECHNOLOGIES, INC. CITRAPURE | KPO | 2006-11-17 | View |
| 510(k) | K023985 | ACIDIFIED COMPONENT CONCENTRATES FOR BICARBONATE DIALYSIS CONTAINING DI-ACETATE | KPO | 2003-02-28 | View |
| 510(k) | K022521 | BICARBONATE DIALYSATE CONCENTRATE MIXER, MODEL 50 GALLON & 100 GALLON | KPO | 2003-01-03 | View |
| 510(k) | K022500 | DRI-SATE DRY ACID CONCENTRATE FOR BICARBONATE DIALYSATE | KPO | 2002-12-23 | View |
| 510(k) | K983618 | DRI-SATE MIXER FOR PREPARATION OF ACIDIFIED DIALYSATE CONCENTRATE | KPO | 1999-08-05 | View |
No matching devices.
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