Mivi Neuroscience, Inc. is one of 16105 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mivi Neuroscience, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Q Distal Access Catheter, MIVI Q Distal Access Catheter, 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
5
Total
5
Cleared
0
Denied
Mivi Neuroscience, Inc. has 5 FDA 510(k) cleared medical devices. Based in Eden Prarie, US.
Last cleared in 2023. Active since 2015. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Mivi Neuroscience, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Philbrook Corporation as regulatory consultant.
FDA 510(k) Regulatory Record - Mivi Neuroscience, Inc.
5 devices
Cleared
Sep 19, 2023
Q Distal Access Catheter
Neurology
357d
Cleared
Dec 16, 2021
MIVI Q Distal Access Catheter
Neurology
136d
Cleared
Apr 06, 2017
MIVI 6F 25cm Mi-EXT Extension Catheter, MIVI 5F 25cm Mi-EXT Extension...
Cardiovascular
140d
Cleared
Dec 09, 2015
MIVI Mi-AXUS Guide Catheter
Cardiovascular
197d
Cleared
Nov 16, 2015
Viradius Neurowire
Neurology
133d