Brightwater Medical
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2019-03-14
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K181669 | ConvertX Biliary Stent System | FGE | 2019-03-14 | View |
| 510(k) | K161277 | ConvertX Nephroureteral Stent System | FAD | 2016-11-22 | View |
No matching devices.