Di-Chem, Inc.
FDA 510(k) & PMA Approved Devices — 6 products
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Total Devices6
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K202508 | Hemo-Lyte C Cartridge | KPO | 2022-08-12 | View |
| 510(k) | K171015 | Citryte | KPO | 2017-10-13 | View |
| 510(k) | K012328 | HEMO-LYTE HEMODIALYSIS GRADE SODIUM BICARBONATE POWDER | KPO | 2002-01-18 | View |
| 510(k) | K012547 | HEMO-LYTE HEMODIALYSIS GRADE SODIUM BICARBONATE SOLUTION | KPO | 2002-01-18 | View |
| 510(k) | K905217 | FORMASURE TEST REAGENT | LIF | 1991-04-09 | View |
| 510(k) | K823103 | DIALYSATE ADDITIVES-POWDER/LIQUID | KPO | 1982-11-17 | View |
No matching devices.
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