Asahi Medical Co., Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Asahi Medical Co., Ltd. - FDA 510(k) Cleared Devices
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
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
Aug 08, 1990
MODIFIED SEPACELL R-SERIES BLOOD FILTERS
General Hospital
104d
Cleared
Jan 24, 1990
MODIFIED SEPACELL PL-SERIES LEUKOCYTE REMOVAL FILT
General Hospital
61d
Cleared
Jan 24, 1990
MODIFIED SEPACELL R-500 AND R-500A BLOOD FILTERS
General Hospital
42d
Cleared
May 18, 1989
NEW AM-SERIES DIALYZERS
Gastroenterology & Urology
48d
Cleared
May 18, 1989
MODIFIED AM-SERIES DIALYZERS
Gastroenterology & Urology
48d