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General Equipment For Medical Imaging (Oncovision-
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K162052 | Sentinella 102, Sentinella 102 Horus | August 18, 2016 |
| K143156 | Sentinella 102; Sentinella 102 Horus | November 18, 2014 |
| K140996 | MAMMI | June 11, 2014 |