FDA 510(k) Applications Submitted by Venclose, Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K160754 | 03/18/2016 | Venclose Radiofrequency System (digiRF Generator, EVSRF Catheter) | VENCLOSE, INC. |
| K211806 | 06/11/2021 | Venclose digiRF Generator with Maven Catheter, Venclose Maven System, Venclose digiRF Generator, Venclose Maven Catheter | Venclose, Inc. |
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