Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Tokotu Electric Co., 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) |
|---|---|---|---|---|---|
| K081242 | 21.3 INCH (53CM) MONOCHROME DIGITAL MAMMOGRAPHY LCD MONITOR | Tokotu Electric Co., Ltd. | 2008-06-11 | 41 | 0 |
| K061061 | 20.1-INCH (51CM) COLOR LCD MONITOR CDL2009A (CCL204) | Tokotu Electric Co., Ltd. | 2006-06-07 | 51 | 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