Dk Medical Technology Co., 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 |
|---|
| K242254 | D·Kutting LL Peripheral Scoring Balloon Dilatation Catheter | April 21, 2025 |
| K232207 | D·Kutting PTA Scoring Balloon Dilatation Catheter | March 7, 2024 |
| K214009 | D·Kaptain PTA High Pressure Balloon Dilatation Catheter | April 5, 2023 |