Medical Mesh Nebulizer (AirICU Max+)
Mar 2026
293d
AIRICU, Inc.
1
Total
1
Cleared
0
Denied
AIRICU, Inc. — FDA 510(k) Submissions
AIRICU, Inc. has submitted 1 FDA 510(k) premarket notifications since 2026, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Ventilator-compatible Nebulizer . Use the specialty filter in the sidebar to narrow results.
1 devices