AXINON? LDL-p Test System
Jul 2023
854d
Numares AG
1
Total
1
Cleared
0
Denied
Numares AG — FDA 510(k) Submissions
Numares AG 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, Test, Low Density, Lipoprotein . Use the specialty filter in the sidebar to narrow results.
1 devices