Medcaptain Life Science Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K230528 | Extension Set | December 1, 2023 |
| K213004 | Needle Free Connector | May 10, 2022 |
| K202578 | KardiFlex NC Coronary Dilatation Catheter | May 6, 2021 |
| K202619 | KardiFlex PTCA Balloon Dilatation Catheter | April 29, 2021 |
| K202748 | Enteral Feeding Catheter | April 9, 2021 |