Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
St. Jude Medical, Daig Division, Inc. · Predicate Candidate Screening
2 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K051096 | APEEL CS PLUS CATHETER DELIVERY SYSTEM, MODELS 407579, 40758 | St. Jude Medical, Daig Division, Inc. | 2005-05-17 | 18 | 0 |
| K042623 | AGILIS STEERABLE CATHETER INTRODUCER, MODEL 408304 | St. Jude Medical, Daig Division, Inc. | 2005-01-27 | 122 | 1 |
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