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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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