Jms Co., Ltd. - FDA 510(k) Cleared Devices
24
Total
24
Cleared
0
Denied
FDA 510(k) Regulatory Record - Jms Co., Ltd. Gastroenterology & Urology ✕
14 devices
Cleared
Sep 06, 2001
JMS A.V. FISTULA NEEDLE SET ACCORDION TYPE
Gastroenterology & Urology
400d
Cleared
Apr 10, 2000
MODIFICATION TO JMS APHERESIS NEEDLE
Gastroenterology & Urology
26d
Cleared
Apr 10, 2000
MODIFICATION TO JMS A.V. FISTULA NEEDLE SET
Gastroenterology & Urology
26d
Cleared
Aug 30, 1999
JMS A. V. FISTULA NEEDLE SET
Gastroenterology & Urology
195d
Cleared
Aug 30, 1999
JMS APHERESIS NEEDLE
Gastroenterology & Urology
193d
Cleared
Jan 08, 1999
JMS DIALYZER PRIMING SET
Gastroenterology & Urology
79d
Cleared
Mar 30, 1998
JMS APHERESIS NEEDLE
Gastroenterology & Urology
90d
Cleared
Aug 07, 1997
JMS AV FISTULA NEEDLE
Gastroenterology & Urology
143d
Cleared
Mar 02, 1993
JMS APHERESIS NEEDLE
Gastroenterology & Urology
473d
Cleared
Aug 28, 1991
JMS AV FISTULA NEEDLES
Gastroenterology & Urology
175d
Cleared
Feb 09, 1990
JMS DIALYZER PRIMING SET
Gastroenterology & Urology
127d
Cleared
Mar 16, 1988
JMS APHERESIS NEEDLE
Gastroenterology & Urology
22d