Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
KCD · Predicate Candidate Screening
3 FDA 510(k) clearances under this product code; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K844169 | VOLUMATIC | Glaxo, Inc. | 1984-11-09 | 15 | 0 |
| K822258 | ESOPHAGEAL BOUGIES | Kelleher Corp. | 1982-08-25 | 27 | 0 |
| K800623 | JACKSON ESOPHAGEAL BOUGIE, X-RAY OPAQUE | Pilling Co. | 1980-04-24 | 36 | 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