Zhuhai Pusen Medical Technology 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 |
|---|
| K233778 | Single Use Suction Access Ureteroscope (PU400A, PU411A), Single Use Flexible Video Ureteroscope (PU3 | July 16, 2024 |
| K223741 | Pusen Single Use Flexible Video Cystoscope/Choledochoscope System (Single Use Flexible Video Cystosc | June 22, 2023 |
| K222602 | Pusen Single Use Flexible Video Cystoscope System (Single Use Flexible Video Cystoscope: PC200-AS, P | September 26, 2022 |
| K190648 | Pusen Eview Medical Video Endoscope Image Processor | March 29, 2019 |
| K172098 | Medical Video Endoscope System | August 31, 2017 |
| K171076 | Medical Video Endoscope System | May 5, 2017 |