Kenota 1 Total IgE; Kenota 1 (instrument)
May 2024
403d
Kenota, Inc.
1
Total
1
Cleared
0
Denied
Kenota, Inc. — FDA 510(k) Submissions
Kenota, Inc. 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 Ige, Antigen, Antiserum, Control . Use the specialty filter in the sidebar to narrow results.
1 devices