Tianjin Medis Medical Device Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 3
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K190274 | Endotracheal Tube | July 30, 2019 |
| K182548 | Accucuff Cuff Pressure Indicator | January 25, 2019 |
| K160694 | Disposable Endotracheal tube, sterile, AccuCuff | April 7, 2017 |