Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Mindray North America · 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) |
|---|---|---|---|---|---|
| K132037 | VITAL SIGNS MONITOR | Mindray North America | 2014-05-16 | 319 | 0 |
| K132038 | ACCUTORR 7 VITAL SIGNS MONITOR | Mindray North America | 2014-05-02 | 305 | 0 |
| K132075 | PASSPORT M SERIES PATIENT MONITORING (INCLUDING MODELS PASSP | Mindray North America | 2014-04-18 | 289 | 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