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FDA 510(k) Applications Submitted by AIROS Medical, Inc.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K172770
09/14/2017
AIROS 6 Sequential Compression Device
AIROS Medical, Inc.
K172779
09/14/2017
AIROS 8 Sequential Compression Device
AIROS Medical, Inc.
K193068
11/04/2019
AIROS 8 Sequential Compression Device
AIROS Medical, Inc.
K193069
11/04/2019
AIROS 6 Sequential Compression Device
AIROS Medical, Inc.
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