Rejoni Intrauterine Catheter
Dec 2022
91d
Rejoni, Inc.
1
Total
1
Cleared
0
Denied
Rejoni, Inc. — FDA 510(k) Submissions
Rejoni, Inc. has submitted 1 FDA 510(k) premarket notifications since 2022, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Cannula, Manipulator/injector, Uterine . Use the specialty filter in the sidebar to narrow results.
1 devices