Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Worldwide 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) |
|---|---|---|---|---|---|
| K912270 | POLYCATH #WMC-900 | Worldwide Medical | 1992-08-05 | 441 | 0 |
| K894401 | BALLOON THERMODILUTION CATHETERS | Worldwide Medical | 1990-04-19 | 304 | 0 |
| K891843 | RANK PATIENT EXAM GLOVES (MFG. INTER-CONTINENTAL) | Worldwide Medical | 1989-06-06 | 71 | 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