Asahi Medical Co., Ltd.
Asahi Medical Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 1983, most recent 2004.
Top product codes for Asahi Medical Co., Ltd.
Recent clearances by Asahi Medical Co., Ltd.
- K041726 — HIGH FLUX HEMODIALYSIS MEMBRANE DIALYZER OR HIGH FLUX HOLLOW FIBER DIALYZER, MODELS APS-R, -M, -S, -E, AND -EX
- K013418 — AM-BIO EXTENDED RANGE SERIES DIALYZER, MODELS WET AND DRY
- K001250 — APS SERIES DIALYZERS (WET MODELS), APS SERIES DIALYSIS (DRY MODELS)
- K991512 — ASAHI AM-R-SERIES DIALYZERS (MODIFIED), MODEL AM-NR-X
- 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-
- K970650 — ASAHI AM-R SERIES DIALYZERS
- K914020 — MODIFIED ASAHI PAN-SERIES HEMOFILTERS
- K901887 — MODIFIED SEPACELL R-SERIES BLOOD FILTERS
- K896664 — MODIFIED SEPACELL PL-SERIES LEUKOCYTE REMOVAL FILT
- K896976 — MODIFIED SEPACELL R-500 AND R-500A BLOOD FILTERS
- K892374 — NEW AM-SERIES DIALYZERS
- K892375 — MODIFIED AM-SERIES DIALYZERS
- K885017 — HEMOSORBA CH-500, CH-350 AND CH-180
- K854575 — MODIFIED AM-SERIES DIALYZERS
- K844663 — ASAHI NEW PAN-SERIES HEMOFILTERS
- K833150 — ASAHI HOLLOW FIBER KIDNEYS, EXCEL
Data sourced from openFDA. This site is unofficial and independent of the FDA.