Kaneka Pharma America, LLC
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K192068 | i-ED COIL | April 25, 2020 |
| K170247 | Lacriflow CL | April 18, 2017 |
| K121301 | XPRESSWAY RX CATHETER (6F LD-VERISON) | July 30, 2012 |
| K101839 | KANEKA PHARMA AMERICA XPRESS-WAY RX | October 22, 2010 |