AIROS 6 Sequential Compression Device

by Airos Medical Inc 510(k)

Active United States

510(k) K193069

Regulatory status

as of 28 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Special	NumberK193069	Date4 Dec 2019Cleared	StatusActive

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

510(k)

510(k) Number: K193069
FDA Product Code: JOW
FDA applicant: Airos Medical, Inc.

Device Class: Class II
Regulation: 21 CFR Part 870.5800
Advisory Committee: Cardiovascular
FDA Decision: SESE Substantially Equivalent

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