Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Daehan Medical Systems 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) |
|---|---|---|---|---|---|
| K180232 | DAEHAN Disposable CUP Electrodes | Daehan Medical Systems Co., Ltd. | 2019-04-03 | 429 | 0 |
| K180247 | DAEHAN Adhesive Surface Electrodes | Daehan Medical Systems Co., Ltd. | 2018-11-01 | 276 | 0 |
| K161566 | DMS Disposable Subdermal Needle Electrodes | Daehan Medical Systems Co., Ltd. | 2016-12-21 | 198 | 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