Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Okami Medical · 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) |
|---|---|---|---|---|---|
| K220383 | LOBO Vascular Occlusion System (models LOBO-7 and LOBO-9) | Okami Medical | 2022-04-29 | 78 | 0 |
| K203025 | LOBO Vascular Occlusion System (model LOBO-5) | Okami Medical | 2020-11-05 | 34 | 0 |
| K192083 | Okami Medical LOBO Vascular Occlusion System | Okami Medical | 2019-10-30 | 89 | 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