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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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