Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Inhalation Therapy Equipment, Co. · 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) |
|---|---|---|---|---|---|
| K821191 | STER-O-MIST 1000 ML | Inhalation Therapy Equipment, Co. | 1982-05-13 | 16 | 0 |
| K820128 | UNI-SET | Inhalation Therapy Equipment, Co. | 1982-03-23 | 64 | 0 |
| K820227 | STER-O-DOSE | Inhalation Therapy Equipment, Co. | 1982-02-23 | 27 | 3 |
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