Home / Companies / Airos Medical, Inc.

Airos Medical, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K240499ARTAIRA Arterial Compression Device (AACD01)October 11, 2024
K223193AIROS 8P Sequential Compression DeviceDecember 9, 2022
K223195AIROS 6P Sequential Compression DeviceDecember 9, 2022
K193068AIROS 8 Sequential Compression DeviceDecember 4, 2019
K193069AIROS 6 Sequential Compression DeviceDecember 4, 2019
K172779AIROS 8 Sequential Compression DeviceJune 22, 2018
K172770AIROS 6 Sequential Compression DeviceJune 22, 2018