Merlin Aspiration System
Jan 2022
56d
Mivi Neurovascular, Inc.
1
Total
1
Cleared
0
Denied
Mivi Neurovascular, Inc. — FDA 510(k) Submissions
Mivi Neurovascular, Inc. has submitted 1 FDA 510(k) premarket notifications since 2022, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Catheter, Embolectomy . Use the specialty filter in the sidebar to narrow results.
1 devices