# Airsonett AB

- Location (FDA's records): Fridley, MN
- FDA decisions: 2 (2008–2013): 2 510(k) clearances
- Names in FDA's records: Airsonett AB (1); Airsonett, Inc. (1)
- Product codes: FRF (2)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 1 (1 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
- Respiraid, Ltd.: 2 (https://510kreport.com/company/respiraid)

## Its most-cited devices
- K081062: Airsonnett Airshower Air 3 (2008), cited by 1

## Recent decisions
- K130702: Airsonett Air-4 (Jul 23, 2013)
- K081062: Airsonnett Airshower Air 3 (Nov 7, 2008)

Source page: https://510kreport.com/company/airsonett