Airehealth, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Airehealth, Inc. - FDA 510(k) Cleared Devices
Recent clearances: AireHealth NebulizerTM
1
Total
1
Cleared
0
Denied
Airehealth, Inc. has 1 FDA 510(k) cleared medical devices. Based in Orlando, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Airehealth, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory and Quality Solutions, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Airehealth, Inc.
1 devices