APEX 6
Mar 2023
421d
Rf Innovations, Inc.
1
Total
1
Cleared
0
Denied
Rf Innovations, Inc. — FDA 510(k) Submissions
Rf Innovations, Inc. 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 Generator, Lesion, Radiofrequency . Use the specialty filter in the sidebar to narrow results.
1 devices