Haolang Medical USA Corporation
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K241581 | Hemodialysis Catheter | May 16, 2025 |
| K201726 | Arterial Catheter | July 7, 2021 |
| K201697 | Umbilical Vessels Catheter | May 6, 2021 |