Arkis Biosciences, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Arkis Biosciences, Inc. has 1 FDA 510(k) cleared medical devices. Based in Knoxville, US.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Arkis Biosciences, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Arkis Biosciences, Inc.
1 devices