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

FDA 510(k) Number Submission Date Device Name Applicant
K212324 07/26/2021 RenovoCath RenovoRx, Inc.
K160067 01/13/2016 RenovoCath RenovoRx, Inc.
K191606 06/17/2019 RenovoCath RenovoRx, Inc.
K141175 05/06/2014 RENOVOCATH RC120 RENOVORX, INC.


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