Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Innomed Technologies, Inc./Respcare, Inc. · Predicate Candidate Screening
2 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K090804 | NASAL AIRE II PEDIATRIC, MODEL 5 SIZES, MODEL TBD | Innomed Technologies, Inc./Respcare, Inc. | 2009-11-05 | 225 | 0 |
| K062019 | RESPCARE HYBRID NE FACE MASK, MODEL TBD,; DISPOSABLE, MODEL | Innomed Technologies, Inc./Respcare, Inc. | 2006-08-17 | 31 | 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