Vista AI, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Vista AI, Inc. has 1 FDA 510(k) cleared medical devices. Based in Palo Alto, US.
Latest FDA clearance: Aug 2025. Active since 2025. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Vista AI, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Heartvista, Inc. Dba Vista.Ai as regulatory consultant.
1 devices