FDA 510(k) Applications Submitted by CROSPON LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K160725 | 03/16/2016 | EndoFLIP | CROSPON LTD. |
| K170833 | 03/20/2017 | EndoFLIP« System with FLIP Topography module | Crospon Ltd. |
| K172128 | 07/14/2017 | EsoFLIP« ES-310 Balloon Catheter | Crospon Ltd. |
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