Kaneka Pharma America, LLC
FDA 510(k) & PMA Approved Devices — 4 products
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Total Devices4
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K192068 | i-ED COIL | HCG | 2020-04-25 | View |
| 510(k) | K170247 | Lacriflow CL | OKS | 2017-04-18 | View |
| 510(k) | K121301 | XPRESSWAY RX CATHETER (6F LD-VERISON) | QEZ | 2012-07-30 | View |
| 510(k) | K101839 | KANEKA PHARMA AMERICA XPRESS-WAY RX | QEZ | 2010-10-22 | View |
No matching devices.
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