Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Meridian Medical Technologies , 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) |
|---|---|---|---|---|---|
| K011058 | TELEPRESS III BLOOD PRESSURE MONITOR, MODEL TPIII | Meridian Medical Technologies , Ltd. | 2001-10-23 | 200 | 0 |
| K010794 | BRIDGE III RECEIVER | Meridian Medical Technologies , Ltd. | 2001-05-10 | 55 | 0 |
| K002310 | CARDIOBEEPER CB12/12, MODEL CB12/12 | Meridian Medical Technologies , Ltd. | 2000-10-25 | 86 | 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