Uro-1, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories2
Latest FDA decision2022-12-02
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K220611 | SUREcore Plus Biopsy Instrument | KNW | 2022-12-02 | View |
| 510(k) | K201650 | VMCore Biopsy Needle | KNW | 2021-01-15 | View |
| 510(k) | K180214 | Repris Bladder Injection System | FBK | 2018-05-03 | View |
No matching devices.