Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Bypass , Ltd. — 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) |
|---|---|---|---|---|---|
| K020470 | MODIFICATION TO CORLINK AUTOMATED ANASTOMOTIC DEVICE | Bypass , Ltd. | 2002-03-08 | 24 | 0 |
| K011589 | CORLINK AAD (3.5 TO 6.0 M M OUTER DIAMETER VESSELS),MODEL 20 | Bypass , Ltd. | 2001-12-26 | 217 | 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