Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Vickers , Ltd. — Predicate Candidate Screening
5 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
138 daysmedian FDA review time
172 days90th percentile
5clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K870330 | SP55 SYRINGE PUMP | Vickers , Ltd. | 1987-06-15 | 138 | 0 |
| K870279 | VP2000 INFUSION PUMP | Vickers , Ltd. | 1987-03-25 | 57 | 0 |
| K854597 | VICKERS MEDICAL MODEL 271 HEART RATE MONITOR | Vickers , Ltd. | 1986-05-09 | 172 | 0 |
| K854598 | VICKERS MEDICAL MODEL 272 TEMPERATURE MONITOR | Vickers , Ltd. | 1986-04-07 | 140 | 0 |
| K854599 | VICKERS MEDICAL MODEL 273 OXYGEN MONITOR | Vickers , Ltd. | 1985-11-27 | 9 | 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