MeMed Diagnostics, Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K230944 | MeMed BV | June 30, 2023 |
| K222332 | MeMed BV | March 23, 2023 |
| K210254 | MeMed BV | September 1, 2021 |