Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Olympus Corp of America · 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) |
|---|---|---|---|---|---|
| K984255 | OLYMPUS HX-20 SERIES LIGATING DEVICE | Olympus Corp of America | 1999-01-12 | 43 | 0 |
| K944250 | UREA NITROGEN REAGENT | Olympus Corp of America | 1995-02-08 | 160 | 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