OVES CERVICAL CAP
Mar 2000
120d
Veos , Ltd.
1
Total
0
Cleared
0
Denied
Veos , Ltd. — FDA 510(k) Submissions
Veos , Ltd. has submitted 1 FDA 510(k) premarket notifications since 2000, of which 0 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Cap, Cervical . Use the specialty filter in the sidebar to narrow results.
1 devices