Minnetronix Neuro, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Minnetronix Neuro, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MindsEye Expandable Port
1
Total
1
Cleared
0
Denied
Minnetronix Neuro, Inc. has 1 FDA 510(k) cleared medical devices. Based in St Paul, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Minnetronix Neuro, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Minnetronix Neuro, Inc.
1 devices