Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Little Doctor Electronic (Nantong)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) |
|---|---|---|---|---|---|
| K193259 | Aneroid sphygmomanometer with stethoscope, Aneroid sphygmoma | Little Doctor Electronic (Nantong)Co.,Ltd | 2020-07-02 | 219 | 0 |
| K123800 | WRIST AUTOMATIC BLOOD PRESSURE MONITOR | Little Doctor Electronic (Nantong)Co.,Ltd | 2013-05-15 | 156 | 0 |
| K123600 | DIGITAL BLOOD PRESSURE MONITOR | Little Doctor Electronic (Nantong)Co.,Ltd | 2013-05-03 | 163 | 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