Mid-America Medical Innovations, LLC is one of 4738 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mid-America Medical Innovations, LLC - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Mid-America Medical Innovations, LLC has 2 FDA 510(k) cleared medical devices. Based in Jefferson City, US.
Historical record: 2 cleared submissions from 2014 to 2016. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Mid-America Medical Innovations, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mid-America Medical Innovations, LLC
2 devices