Crospon, Ltd.
FDA 510(k) & PMA Approved Devices — 11 products
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Total Devices11
Categories0
Latest FDA decision
| 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 |
| 510(k) | K132337 | ESOFLIP BALLOON DILATION CATHETER | PID | 2013-10-07 | View |
| 510(k) | K130906 | ENDOFLIP CATHETER | FFX | 2013-07-17 | View |
| 510(k) | K120997 | BAROSTAT SOFTWARE OPTION | FFX | 2012-08-27 | View |
| 510(k) | K110531 | ENDOFLIP ECD | FED | 2011-10-06 | View |
| 510(k) | K110529 | ENDOFLIP GASTRIC TUBE | KNT | 2011-07-22 | View |
| 510(k) | K102214 | ENDO FLIP | FFX | 2010-12-16 | View |
| 510(k) | K092850 | ENDOFLIP | FFX | 2009-12-15 | View |
No matching devices.
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