Nucleix , Ltd.
FDA 510(k) & PMA Approved Devices — 1 products
Total Devices1
Categories1
Latest Approval2023-05-04
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K203245 | Bladder EpiCheck DNA extraction kit, NX899090-01C, Bladder EpiCheck test kit, NX899090-02C, Bladder EpiCheck Software, NX899090-03C | MMW | 2023-05-04 | View |
No matching devices.