Kaneka Pharma America, LLC - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Kaneka Pharma America, LLC has 4 FDA 510(k) cleared medical devices. Based in Hudson, US.
Historical record: 4 cleared submissions from 2010 to 2020. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Kaneka Pharma America, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Kaneka Pharma America, LLC
4 devices