Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Khi, Inc. · Predicate Candidate Screening
4 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K830404 | RAD VALVE | Khi, Inc. | 1983-03-17 | 38 | 0 |
| K830399 | COUPLING/VALVE | Khi, Inc. | 1983-03-10 | 31 | 0 |
| K811858 | KHI CPRAM BREATHING CIRCUIT | Khi, Inc. | 1981-07-16 | 15 | 0 |
| K800456 | EMERGIENCY RESUSCITATOR/INHALOR W/ASPIR. | Khi, Inc. | 1980-03-18 | 18 | 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