Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Aerogen Ireland, Ltd. — Predicate Candidate Screening
3 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K102240 | NIVO NEBULIZER SYSTEM | Aerogen Ireland, Ltd. | 2010-11-10 | 93 | 0 |
| K081650 | AERONEB GO NEBULIZER | Aerogen (Ireland), Ltd. | 2008-10-23 | 133 | 0 |
| K070642 | AERONEB PROFESSIONAL NEBULIZER SYSTEM | Aerogen (Ireland), Ltd. | 2007-05-07 | 60 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda