Daehan Medical Systems Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K180232 | DAEHAN Disposable CUP Electrodes | April 3, 2019 |
| K180247 | DAEHAN Adhesive Surface Electrodes | November 1, 2018 |
| K161566 | DMS Disposable Subdermal Needle Electrodes | December 21, 2016 |