Altris IMS
Jul 2023
18d
Altris, Inc.
1
Total
1
Cleared
0
Denied
Altris, Inc. — FDA 510(k) Submissions
Altris, Inc. has submitted 1 FDA 510(k) premarket notifications since 2023, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include System, Image Management, Ophthalmic . Use the specialty filter in the sidebar to narrow results.
1 devices