FDA 510(k) Applications Submitted by Cerus Endovascular, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K213314 10/04/2021 CerusEndo Microcatheter (027) Cerus Endovascular, Inc.
K182487 09/11/2018 CerusEndo Microcatheter Cerus Endovascular, Inc.


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