Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
DFD · 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) |
|---|---|---|---|---|---|
| K940242 | VENTANA CEA PRIMARY ANTIBODY | Ventana Medical Systems, Inc. | 1996-12-23 | 1069 | 0 |
| K924578 | PSA ANTIBODY KIT | Ventana Medical Systems, Inc. | 1993-02-05 | 148 | 0 |
| K924629 | PAP ANTIBODY KIT | Ventana Medical Systems, Inc. | 1993-02-04 | 143 | 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