Tianjin Rilifine Medical Device Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K222246 | Disposable Sterile Lancet | November 21, 2022 |
| K222055 | Disposable Sterile Lancet | November 15, 2022 |