Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Mytech Technology Co., Ltd. · Predicate Candidate Screening
4 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K061959 | MYTECH / HAPPY LIFE / MAXIAIDS ARM BLOOD PRESSURE MONITOR, H | Mytech Technology Co., Ltd. | 2006-08-22 | 42 | 0 |
| K041228 | MYTECH/HAPPY LIFE BLOOD PRESSURE MONITOR, MODEL HPL-200 | Mytech Technology Co., Ltd. | 2004-05-17 | 7 | 0 |
| K030221 | MYTECH / HAPPY LIFE BLOOD PRESSURE MONITOR | Mytech Technology Co., Ltd. | 2003-07-25 | 185 | 0 |
| K030561 | MYTECH/HAPPY LIFE BLOOD PRESSURE MONITOR, MODELS HPL-100 AND | Mytech Technology Co., Ltd. | 2003-05-09 | 77 | 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