Fenom Pro Nitric Oxide Test
Feb 2019
124d
Spirosure, Inc.
1
Total
1
Cleared
0
Denied
Spirosure, Inc. — FDA 510(k) Submissions
Spirosure, Inc. has submitted 1 FDA 510(k) premarket notifications since 2019, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include System, Test, Breath Nitric Oxide . Use the specialty filter in the sidebar to narrow results.
1 devices