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

FDA 510(k) Number Submission Date Device Name Applicant
K151396 05/26/2015 MIVI Mi-AXUS Guide Catheter MIVI NEUROSCIENCE, INC
K163233 11/17/2016 MIVI 6F 25cm Mi-EXT Extension Catheter, MIVI 5F 25cm Mi-EXT Extension Catheter, MIVI 4F 30cm Mi-EXT Extension Catheter, MIVI 3F 43cm Mi-EXT Extension Catheter MIVI NEUROSCIENCE, INC
K222948 09/27/2022 Q Distal Access Catheter MIVI Neuroscience, Inc


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