Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Avantec Vascular Corp. — Predicate Candidate Screening
3 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K032436 | DURAMAX .018 BILIARY STENT SYSTEM | Avantec Vascular Corp. | 2004-02-04 | 181 | 0 |
| K030638 | DURAMAX .035 BILIARY STENT SYSTEM, MODELS DML0718-80, DML071 | Avantec Vascular Corp. | 2003-07-09 | 131 | 0 |
| K030062 | ADMIRAL .035 DILATATION CATHETER, MODELS ADL0720-80,ADL0720- | Avantec Vascular Corp. | 2003-04-03 | 86 | 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