Asahi Medical Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: HIGH FLUX HEMODIALYSIS MEMBRANE DIALYZER OR HIGH FLUX HOLLOW FIBER DIALYZER, MODELS APS-R, -M, -S, -E, AND -EX, AM-BIO EXTENDED RANGE SERIES DIALYZER, MODELS WET AND DRY, APS SERIES DIALYZERS (WET MODELS), APS SERIES DIALYSIS (DRY MODELS)
16
Total
16
Cleared
0
Denied
FDA 510(k) Regulatory Record - Asahi Medical Co., Ltd. General Hospital ✕
3 devices