FDA 510(k) Applications Submitted by Vygon USA
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K181208 | 05/07/2018 | Vygon Midline 3 Fr SL Catheter; Vygon Midline 4 Fr SL Catheter; Vygon Midline 5 Fr DL Catheter | Vygon USA |
| K172899 | 09/22/2017 | Vygon PICCs | Vygon USA |
| K212370 | 07/30/2021 | Leaderflex Mini and Leaderflex Nano | Vygon USA |
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