Silq Technologies Corporation
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 2
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K233013 | 2-Way 100% Silicone Cleartract Catheter | January 23, 2024 |
| K221625 | 2-Way 100% Silicone ClearTract Catheter | July 1, 2022 |