Asahi Kasei Medical Co., Ltd.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2026-04-09
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| PMA | P820033 | Separator for therapeutic purposes, membrane automated blood cell/plasma | MDP | 2026-04-09 | View |
| 510(k) | K162248 | Asahi ViE-U Series Dialyzer | KDI | 2017-05-03 | View |
No matching devices.