Cary
May 2025
26d
Excitus AS
1
Total
1
Cleared
0
Denied
Excitus AS — FDA 510(k) Submissions
Excitus AS has submitted 1 FDA 510(k) premarket notifications since 2025, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Apparatus, Suction, Ward Use, Portable, Ac-powered . Use the specialty filter in the sidebar to narrow results.
1 devices