The Flume Catheter Company, Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K231101 | Flume Catheter | June 29, 2023 |
| K212151 | FLUME catheter | November 3, 2021 |