Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Mianyang Meike Electronic Equipment Co., 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) |
|---|---|---|---|---|---|
| K210591 | Palm Bladder Scanner - PBSV7.1 | Mianyang Meike Electronic Equipment Co., Ltd. | 2021-06-09 | 100 | 0 |
| K191307 | Palm Bladder Scanner - PBSV5.1 | Mianyang Meike Electronic Equipment Co., Ltd. | 2019-06-05 | 22 | 0 |
| K130229 | PALM BLADDER SCANNER | Mianyang Meike Electronic Equipment Co., Ltd. | 2013-03-20 | 50 | 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