FDA 510(k) Applications Submitted by Venclose, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K250068 01/10/2025 Venclose digiRF Generator (VCRFG1) Venclose, Inc.
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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