Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
DKA · 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) |
|---|---|---|---|---|---|
| K934003 | STRATUS DIGOXIN FLOUROMETRIC ENZYME IMMUNOASSAY | Baxter Diagnostics, Inc. | 1994-11-22 | 462 | 0 |
| K780498 | CBR-DIGOXIN ANTISERUM | Clinical Bioresearch | 1978-04-05 | 8 | 0 |
| K780316 | RABBIT ANTIBODY TO DIGOXIN | Pcl-Ria, Inc. | 1978-03-17 | 21 | 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