ProVee Video Processing Unit (PV-003)
Sep 2025
110d
Proverum Limited
1
Total
1
Cleared
0
Denied
Proverum Limited — FDA 510(k) Submissions
Proverum Limited has submitted 1 FDA 510(k) premarket notifications since 2025, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Endoscopic Video Imaging System/component, Gastroenterology-urology . Use the specialty filter in the sidebar to narrow results.
1 devices