FDA 510(k) Applications Submitted by MIVI Neuroscience, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K212402 08/02/2021 MIVI Q Distal Access Catheter MIVI Neuroscience, Inc.
K151825 07/06/2015 Viradius Neurowire MIVI NEUROSCIENCE, INC.


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