Deep Capsule? (Deep Capsule US)
Mar 2026
372d
Digestaid - Artificial Intelligence Development SA
1
Total
1
Cleared
0
Denied
Digestaid - Artificial Intelligence Development SA — FDA 510(k) Submissions
Digestaid - Artificial Intelligence Development SA has submitted 1 FDA 510(k) premarket notifications since 2026, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Gastrointestinal Capsule Endoscopy Analysis Software Device . Use the specialty filter in the sidebar to narrow results.
1 devices