Anrei Medical (Hangzhou) Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K212999 | Multi-Functional Electrosurgical Knife | March 21, 2022 |
| K210917 | Single Use Injection Needle | May 28, 2021 |
| K202987 | Rescue Pulmonary Grasping Forceps | April 29, 2021 |
| K210660 | Stone Retrieval Balloon Catheter | April 27, 2021 |
| K201771 | Single Use Rotatable and Repositionable Hemoclip | October 19, 2020 |
| K192048 | Single Use Endoscope Valves Set | May 14, 2020 |