Radialis, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Radialis, Inc. has 1 FDA 510(k) cleared medical devices. Based in Thunder Bay, CA.
Last cleared in 2022. Active since 2022. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Radialis, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Beanstock Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Radialis, Inc.
1 devices