Utepreva Endometrial Sampler (UP01)
Aug 2024
163d
Utepreva, LLC
1
Total
1
Cleared
0
Denied
Utepreva, LLC — FDA 510(k) Submissions
Utepreva, LLC has submitted 1 FDA 510(k) premarket notifications since 2024, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Brush, Endometrial . Use the specialty filter in the sidebar to narrow results.
1 devices