Rovers Medical Devices B.V.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K043369 | CERVEX-BRUSH COMBI | February 2, 2005 |
| K002520 | ROVERS SPATULA | November 13, 2000 |
| K001119 | ROVERS ENDOCERVEX-BRUSH | May 19, 2000 |