Amsel Medical Corporation
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K180650 | Amsel Endo Occluder | November 15, 2018 |
| K140932 | AMSEL OCCLUDER DEVICE | January 23, 2015 |