Medical Device Manufacturer · US , Santa Clara , CA

Exo Imaging

2 submissions · 2 cleared · Since 2024
2
Total
2
Cleared
0
Denied

Exo Imaging — FDA 510(k) Submissions

Exo Imaging has submitted 2 FDA 510(k) premarket notifications since 2024, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Automated Radiological Image Processing Software . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
Filters
All2 Radiology 2