DEKA Research & Development
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories3
Latest FDA decision2020-02-21
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K191313 | Unity Subcutaneous Infusion System for Remodulin | QJY | 2020-02-21 | View |
| 510(k) | K190182 | Unity Subcutaneous Delivery System for Remodulin | FRN | 2019-05-06 | View |
| 510(k) | K153760 | Volumetric Infusion Controller | LDR | 2016-10-03 | View |
No matching devices.