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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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