Airos Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Airos Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ARTAIRA Arterial Compression Device (AACD01), AIROS 8P Sequential Compression Device, AIROS 6P Sequential Compression Device
7
Total
7
Cleared
0
Denied
Airos Medical, Inc. has 7 FDA 510(k) cleared medical devices. Based in Audubon, US.
Latest FDA clearance: Oct 2024. Active since 2018. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Airos Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Airos Medical, Inc.
7 devices
Cleared
Oct 11, 2024
ARTAIRA Arterial Compression Device (AACD01)
Cardiovascular
234d
Cleared
Dec 09, 2022
AIROS 8P Sequential Compression Device
Cardiovascular
57d
Cleared
Dec 09, 2022
AIROS 6P Sequential Compression Device
Cardiovascular
57d
Cleared
Dec 04, 2019
AIROS 8 Sequential Compression Device
Cardiovascular
30d
Cleared
Dec 04, 2019
AIROS 6 Sequential Compression Device
Cardiovascular
30d
Cleared
Jun 22, 2018
AIROS 6 Sequential Compression Device
Cardiovascular
281d
Cleared
Jun 22, 2018
AIROS 8 Sequential Compression Device
Cardiovascular
281d