Asahi Medical Co., Ltd. - FDA 510(k) Cleared Devices
16
Total
16
Cleared
0
Denied
FDA 510(k) Regulatory Record - Asahi Medical Co., Ltd. Gastroenterology & Urology ✕
13 devices
Cleared
Jul 23, 2004
HIGH FLUX HEMODIALYSIS MEMBRANE DIALYZER OR HIGH FLUX HOLLOW FIBER DIALYZER,...
Gastroenterology & Urology
28d
Cleared
Jul 09, 2002
AM-BIO EXTENDED RANGE SERIES DIALYZER, MODELS WET AND DRY
Gastroenterology & Urology
267d
Cleared
Aug 16, 2000
APS SERIES DIALYZERS (WET MODELS), APS SERIES DIALYSIS (DRY MODELS)
Gastroenterology & Urology
119d
Cleared
Jul 29, 1999
ASAHI AM-R-SERIES DIALYZERS (MODIFIED), MODEL AM-NR-X
Gastroenterology & Urology
90d
Cleared
May 17, 1999
ASAHI AM-BIO SERIES DIALYZERS (WET MODELS)& (DRY MODELS), MODELS...
Gastroenterology & Urology
208d
Cleared
Sep 30, 1997
ASAHI AM-R SERIES DIALYZERS
Gastroenterology & Urology
222d
Cleared
Mar 20, 1992
MODIFIED ASAHI PAN-SERIES HEMOFILTERS
Gastroenterology & Urology
193d
Cleared
May 18, 1989
NEW AM-SERIES DIALYZERS
Gastroenterology & Urology
48d
Cleared
May 18, 1989
MODIFIED AM-SERIES DIALYZERS
Gastroenterology & Urology
48d
Cleared
Mar 17, 1989
HEMOSORBA CH-500, CH-350 AND CH-180
Gastroenterology & Urology
102d
Cleared
Dec 02, 1985
MODIFIED AM-SERIES DIALYZERS
Gastroenterology & Urology
26d
Cleared
Jan 18, 1985
ASAHI NEW PAN-SERIES HEMOFILTERS
Gastroenterology & Urology
49d
Cleared
Nov 15, 1983
ASAHI HOLLOW FIBER KIDNEYS, EXCEL
Gastroenterology & Urology
61d