Medical Device Manufacturer · US , Walker , MI

Asahi Medical Co., Ltd. - FDA 510(k) Cleared Devices

16 submissions · 16 cleared · Since 1983

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

Asahi Medical Co., Ltd. has 16 FDA 510(k) cleared gastroenterology & urology devices. Based in Walker, US.

Historical record: 16 cleared submissions from 1983 to 2004.

Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Asahi Medical Co., Ltd.

16 devices
1-12 of 16
Filters