# K172779: AIROS 8 Sequential Compression Device

- Pathway: 510(k) (Traditional)
- Applicant: Airos Medical, Inc.
- Decided: Jun 22, 2018 after 281 days
- Product code: JOW (Sleeve, Limb, Compressible)
- Device class: 2
- Regulation: 21 CFR 870.5800
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K810338 (1981). 11 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 14 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K123647: Circuflow 5208 Sequential Compression Device, Devon Medical, Inc. (2013) Summary page 4.

## Most influential descendants
- K193068: AIROS 8 Sequential Compression Device (2019), 1 descendant of its own
- K223193: AIROS 8P Sequential Compression Device (2022), 0 descendants of its own

## Indications for use
The AIROS 8 Sequential Compression Device utilizes gradient pneumatic compression, which is intended for treatment of patients with the following conditions: * Lymphedema * Venous stasis ulcers * Venous insufficiency * Peripheral edema The device is safe for both home and hospital use.

Source page: https://510kreport.com/device/K172779
Methodology: https://510kreport.com/methodology