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