# Airos Medical, Inc.

- Location (FDA's records): Audubon, PA
- FDA decisions: 7 (2018–2024): 7 510(k) clearances
- Product codes: JOW (7)
- 510(k) review time since 2016: median 57 days, against 88 for FDA's reviews in the same codes and years (4 of 7 faster)
- Predicates its devices cite: 7 (4 its own); citations of its devices by later devices: 5 (4 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Devon Medical, Inc.: 2 (https://510kreport.com/company/devon-medical)
- Aci Medical, Inc.: 1 (https://510kreport.com/company/aci-medical)

## Firms that cite its devices most
- Biotab, LLC: 1 (https://510kreport.com/company/biotab)

## Its most-cited devices
- K223195: AIROS 6P Sequential Compression Device (2022), cited by 1
- K172779: AIROS 8 Sequential Compression Device (2018), cited by 1
- K193069: AIROS 6 Sequential Compression Device (2019), cited by 1
- K193068: AIROS 8 Sequential Compression Device (2019), cited by 1
- K172770: AIROS 6 Sequential Compression Device (2018), cited by 1

## Recent decisions
- K240499: ARTAIRA Arterial Compression Device (AACD01) (Oct 11, 2024)
- K223195: AIROS 6P Sequential Compression Device (Dec 9, 2022)
- K223193: AIROS 8P Sequential Compression Device (Dec 9, 2022)
- K193069: AIROS 6 Sequential Compression Device (Dec 4, 2019)
- K193068: AIROS 8 Sequential Compression Device (Dec 4, 2019)
- K172779: AIROS 8 Sequential Compression Device (Jun 22, 2018)
- K172770: AIROS 6 Sequential Compression Device (Jun 22, 2018)

Source page: https://510kreport.com/company/airos-medical