# Aerogen (Ireland), Ltd.

- Location (FDA's records): Dangan Galway, IE
- FDA decisions: 3 (2007–2010): 3 510(k) clearances
- Names in FDA's records: Aerogen (Ireland), Ltd. (2); Aerogen Ireland, Ltd. (1)
- Product codes: CAF (3)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Respironics Respiratory Drug Delivery (Uk), Ltd.: 1 (https://510kreport.com/company/respironics-respiratory-drug-delivery-uk)
- Aerogen, Ltd.: 1 (https://510kreport.com/company/aerogen)
- Trudell Medical Intl.: 1 (https://510kreport.com/company/trudell-medical-intl)

## Its most-cited devices
- K070642: Aeroneb Professional Nebulizer System (2007), cited by 2
- K081650: Aeroneb GO Nebulizer (2008), cited by 1

## Recent decisions
- K102240: Nivo Nebulizer System (Nov 10, 2010)
- K081650: Aeroneb GO Nebulizer (Oct 23, 2008)
- K070642: Aeroneb Professional Nebulizer System (May 7, 2007)

Source page: https://510kreport.com/company/aerogen-ireland