Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Op-Co Medical Products , Ltd. · 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) |
|---|---|---|---|---|---|
| K941098 | SECURE-SITE | Op-Co Medical Products , Ltd. | 1995-08-09 | 518 | 0 |
| K932757 | SECURODRIP (TM) I.V. ARMBOARD | Op-Co Medical Products , Ltd. | 1993-12-08 | 187 | 0 |
| K912660 | SECURODRIP | Op-Co Medical Products , Ltd. | 1991-12-04 | 170 | 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