Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Baxter Healthcare Corporation - Renal Division · 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) |
|---|---|---|---|---|---|
| K120443 | NEUTRAL LUER ACTIVATED DEVICE AND EXTENSION SETS WITH NEUTRA | Baxter Healthcare Corporation - Renal Division | 2012-05-22 | 98 | 0 |
| K093120 | XENIUM XPM 110, XENIUM XPM 130, MODELS M25649A, M25650A, XEN | Baxter Healthcare Corporation - Renal Division | 2010-02-17 | 138 | 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