Akura Thrombectomy System
Nov 2025
232d
Akura Medical
1
Total
1
Cleared
0
Denied
Akura Medical — FDA 510(k) Submissions
Akura Medical 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 Peripheral Mechanical Thrombectomy With Aspiration . Use the specialty filter in the sidebar to narrow results.
1 devices