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Ge Medical Systems Ultrasound and Primary Care Diagnostic,
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K231989 | LOGIQ E10s, LOGIQ Fortis | November 7, 2023 |
| K232186 | LOGIQ e | November 3, 2023 |
| K230346 | Voluson SWIFT; Voluson SWIFT+ | June 20, 2023 |