De Soutter Medical, Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 2
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K930784 | THE DE SOUTTER M193 REAMER | October 27, 1993 |
| K930785 | THE DE SOUTTER M182 DRILL | October 27, 1993 |