Tinearity G1 (6103); Tinearity G1 Adapters x3 (6042)
Jun 2023
203d
Duearity AB
1
Total
1
Cleared
0
Denied
Duearity AB — FDA 510(k) Submissions
Duearity AB 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 Masker, Tinnitus . Use the specialty filter in the sidebar to narrow results.
1 devices