Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Shenzhen Yuezhongxing Technology 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) |
|---|---|---|---|---|---|
| K233799 | Wrist Blood Pressure Monitor (222); Wrist Blood Pressure Mon | Shenzhen Yuezhongxing Technology Co., Ltd. | 2024-03-15 | 107 | 0 |
| K222926 | Arm Blood Pressure Monitor, Model Name:111, Arm Blood Pressu | Shenzhen Yuezhongxing Technology Co., Ltd. | 2023-05-05 | 221 | 0 |
| K211041 | Wrist Blood Pressure Monitor, Model Name:W203, Wrist Blood P | Shenzhen Yuezhongxing Technology Co., Ltd. | 2021-08-30 | 144 | 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