Aluna 2
Nov 2024
458d
Knox Medical Diagnostics
1
Total
1
Cleared
0
Denied
Knox Medical Diagnostics — FDA 510(k) Submissions
Knox Medical Diagnostics 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 Meter, Peak Flow, Spirometry . Use the specialty filter in the sidebar to narrow results.
1 devices