Asahi Medical Co., Ltd.
FDA 510(k) medical device clearances.
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.