Easymed Instruments Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K241899 | Pelvic Floor Stimulator (Intrelief PFE) | November 27, 2024 |
| K211263 | Intrelief | December 30, 2021 |
| K140168 | EASYSTIM TN28_OTC | August 28, 2014 |