Suzhou Hengrui Disheng Medical 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 |
|---|
| K193653 | Hydrophilic Coating Guide Wire | August 26, 2020 |
| K193647 | Superpipe Angiographic Catheter | July 29, 2020 |
| K171665 | Microcatheter and guide-wire system | January 11, 2018 |