Company · US
Crospon, Ltd.
FDA 510(k) clearances and medical device recalls filed under this name, 2009 to 2019. Name variants (Inc, Corp, punctuation) are merged.
12510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Feb 15, 2019 | K183072 | EndoFLIP System Crospon, Ltd., IE | FFX |
| Nov 22, 2017 | K172128 | EsoFLIP® ES-310 Balloon Catheter Crospon, Ltd., IE | PIE |
| Apr 17, 2017 | K170833 | EndoFLIP® System with FLIP Topography module Crospon, Ltd., IE | FFX |
| May 1, 2016 | K160725 | EndoFLIP Crospon, Ltd., IE | FFX |
| Sep 25, 2014 | K142000 | ESOFLIP ES Crospon, Ltd. | PIE |
| Oct 7, 2013 | K132337 | ESOFLIP BALLOON DILATION CATHETER Crospon, Ltd. | PID |
| Jul 17, 2013 | K130906 | ENDOFLIP CATHETER Crospon, Ltd. | FFX |
| Aug 27, 2012 | K120997 | BAROSTAT SOFTWARE OPTION Crospon, Ltd. | FFX |
| Oct 6, 2011 | K110531 | ENDOFLIP ECD Crospon, Ltd. | FED |
| Jul 22, 2011 | K110529 | ENDOFLIP GASTRIC TUBE Crospon, Ltd. | KNT |
| Dec 16, 2010 | K102214 | ENDO FLIP Crospon, Ltd. | FFX |
| Dec 15, 2009 | K092850 | ENDOFLIP Crospon, Ltd. | FFX |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||