Asahi Medical Co., Ltd.
FDA 510(k) & PMA Approved Devices — 16 products
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Total Devices16
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K041726 | HIGH FLUX HEMODIALYSIS MEMBRANE DIALYZER OR HIGH FLUX HOLLOW FIBER DIALYZER, MODELS APS-R, -M, -S, -E, AND -EX | KDI | 2004-07-23 | View |
| 510(k) | K013418 | AM-BIO EXTENDED RANGE SERIES DIALYZER, MODELS WET AND DRY | KDI | 2002-07-09 | View |
| 510(k) | K001250 | APS SERIES DIALYZERS (WET MODELS), APS SERIES DIALYSIS (DRY MODELS) | KDI | 2000-08-16 | View |
| 510(k) | K991512 | ASAHI AM-R-SERIES DIALYZERS (MODIFIED), MODEL AM-NR-X | FJI | 1999-07-29 | View |
| 510(k) | K983720 | ASAHI AM-BIO SERIES DIALYZERS (WET MODELS)& (DRY MODELS), MODELS AM-BIO-50,AM-BIO-65, AM-BIO-75, AND AM-BIO-100, AM-BIO- | MSE | 1999-05-17 | View |
| 510(k) | K970650 | ASAHI AM-R SERIES DIALYZERS | MSE | 1997-09-30 | View |
| 510(k) | K914020 | MODIFIED ASAHI PAN-SERIES HEMOFILTERS | KDI | 1992-03-20 | View |
| 510(k) | K901887 | MODIFIED SEPACELL R-SERIES BLOOD FILTERS | CAK | 1990-08-08 | View |
| 510(k) | K896664 | MODIFIED SEPACELL PL-SERIES LEUKOCYTE REMOVAL FILT | CAK | 1990-01-24 | View |
| 510(k) | K896976 | MODIFIED SEPACELL R-500 AND R-500A BLOOD FILTERS | CAK | 1990-01-24 | View |
| 510(k) | K892374 | NEW AM-SERIES DIALYZERS | FJI | 1989-05-18 | View |
| 510(k) | K892375 | MODIFIED AM-SERIES DIALYZERS | FJI | 1989-05-18 | View |
| 510(k) | K885017 | HEMOSORBA CH-500, CH-350 AND CH-180 | FLD | 1989-03-17 | View |
| 510(k) | K854575 | MODIFIED AM-SERIES DIALYZERS | FJI | 1985-12-02 | View |
| 510(k) | K844663 | ASAHI NEW PAN-SERIES HEMOFILTERS | KDI | 1985-01-18 | View |
| 510(k) | K833150 | ASAHI HOLLOW FIBER KIDNEYS, EXCEL | KOC | 1983-11-15 | View |
No matching devices.
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