Tsk Laboratory International Japan KK
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K242073 | STERiJECT Ophthalmic Needle; STERiJECT Ophthalmic Needle Low Dead Space (LDS) | October 23, 2024 |
| K231734 | STERiJECT Low Dead Space, STERiJECT The Invisible Needle | March 8, 2024 |