Crospon, Ltd.
12 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| EndoFLIP System (K183072) | Crospon, Ltd. | 2019-02-15 |
| EsoFLIP® ES-310 Balloon Catheter (K172128) | Crospon, Ltd. | 2017-11-22 |
| EndoFLIP® System with FLIP Topography module (K170833) | Crospon, Ltd. | 2017-04-17 |
| EndoFLIP (K160725) | Crospon, Ltd. | 2016-05-01 |
| ESOFLIP ES (K142000) | Crospon, Ltd. | 2014-09-25 |
| ESOFLIP BALLOON DILATION CATHETER (K132337) | Crospon, Ltd. | 2013-10-07 |
| ENDOFLIP CATHETER (K130906) | Crospon, Ltd. | 2013-07-17 |
| BAROSTAT SOFTWARE OPTION (K120997) | Crospon, Ltd. | 2012-08-27 |
| ENDOFLIP ECD (K110531) | Crospon, Ltd. | 2011-10-06 |
| ENDOFLIP GASTRIC TUBE (K110529) | Crospon, Ltd. | 2011-07-22 |
| ENDO FLIP (K102214) | Crospon, Ltd. | 2010-12-16 |
| ENDOFLIP (K092850) | Crospon, Ltd. | 2009-12-15 |
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