Z-NET
Dec 2001
621d
Demite Limited
1
Total
1
Cleared
0
Denied
Demite Limited — FDA 510(k) Submissions
Demite Limited has submitted 1 FDA 510(k) premarket notifications since 2001, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Cover, Mattress (medical Purposes) . Use the specialty filter in the sidebar to narrow results.
1 devices