Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Ashitaka Factory of Terumo Corporation · 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) |
|---|---|---|---|---|---|
| K203521 | FineCross M3 | Ashitaka Factory of Terumo Corporation | 2021-03-03 | 92 | 0 |
| K170223 | Progreat | Ashitaka Factory of Terumo Corporation | 2017-07-21 | 177 | 0 |
| K161546 | R2P SlenGuide | Ashitaka Factory of Terumo Corporation | 2016-10-14 | 133 | 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