PanopticAI technologies Limited - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
PanopticAI technologies Limited has 1 FDA 510(k) cleared medical devices. Based in Hong Kong, HK.
Latest FDA clearance: Dec 2024. Active since 2024. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by PanopticAI technologies Limited Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Vee Care (Asia) Limited as regulatory consultant.
1 devices