Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Shenzhen Kingyield Technology Co., Ltd. · Predicate Candidate Screening
5 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
169 daysmedian FDA review time
302 days90th percentile
5clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K182018 | Bluetooth blood pressure monitor | Shenzhen Kingyield Technology Co., Ltd. | 2018-10-06 | 71 | 0 |
| K161530 | Bluetooth blood pressure monitor | Shenzhen Kingyield Technology Co., Ltd. | 2017-03-31 | 302 | 0 |
| K123801 | FINGER PULSE OXIMETER | Shenzhen Kingyield Technology Co., Ltd. | 2013-05-28 | 169 | 0 |
| K112042 | KINGYIELD WRIST BLOOD PRESSURE MONITOR | Shenzhen Kingyield Technology Co., Ltd. | 2012-02-10 | 207 | 0 |
| K083043 | KING`YIELD WRIST BLOOD PRESSURE MONITOR, MODEL BP201 | Shenzhen Kingyield Technology Co., Ltd. | 2008-10-27 | 13 | 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