Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Victus, Inc. — 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) |
|---|---|---|---|---|---|
| K093271 | EXTENSION SET (STANDARDBORE TUBING), EXTENSION SET (MINIBORE | Victus, Inc. | 2010-01-27 | 100 | 0 |
| K030246 | VICTUS I.V. ADMINISTRATION SET, MODELS 27071 AND 27072 | Victus, Inc. | 2003-02-26 | 33 | 0 |
| K023469 | VICTUS I.V. ADMINISTRATION SET, MODELS 27058, 27059,27062 | Victus, Inc. | 2002-12-10 | 55 | 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