Crospon, Ltd.
FDA 510(k) & PMA Approved Devices — 4 products
Total Devices4
Categories2
Latest FDA decision2019-02-15
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K183072 | EndoFLIP System | FFX | 2019-02-15 | View |
| 510(k) | K172128 | EsoFLIP® ES-310 Balloon Catheter | PIE | 2017-11-22 | View |
| 510(k) | K170833 | EndoFLIP® System with FLIP Topography module | FFX | 2017-04-17 | View |
| 510(k) | K160725 | EndoFLIP | FFX | 2016-05-01 | View |
No matching devices.