General Equipment For Medical Imaging, S.A.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K232569 | CAREMIBRAIN | September 21, 2023 |
| K161631 | MAMMI | July 28, 2016 |
| K110601 | SENTINELLA 102 | March 18, 2011 |
| K092471 | MODEL SENTINELLA 102 | October 2, 2009 |