BB 8 Sinus Dilation Kit
May 2023
114d
Excelent, Inc.
1
Total
1
Cleared
0
Denied
Excelent, Inc. — FDA 510(k) Submissions
Excelent, 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 Instrument, Ent Manual Surgical . Use the specialty filter in the sidebar to narrow results.
1 devices