Jms Co., Ltd. is one of 79 FDA 510(k) medical device manufacturers from Japan in the dataset, ranked by real submission volume.
Jms Co., Ltd. - FDA 510(k) Cleared Devices
24
Total
24
Cleared
0
Denied
Jms Co., Ltd. has 24 FDA 510(k) cleared medical devices. Based in Hiroshima, JP.
Historical record: 24 cleared submissions from 1985 to 2001. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Jms Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Jms Co., Ltd.
24 devices
Cleared
Sep 06, 2001
JMS A.V. FISTULA NEEDLE SET ACCORDION TYPE
Gastroenterology & Urology
400d
Cleared
Sep 05, 2001
JMS APHERESIS NEEDLE SET ACCORDION TYPE
General Hospital
394d
Cleared
Jun 20, 2001
JMS A.V. FISTULA NEEDLE SET WING EATER, MODEL 14G-18G
General Hospital
128d
Cleared
Jun 20, 2001
JMS APHERESIS NEEDLE WING EATER, MODEL 14G-18G
General Hospital
128d
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 31, 1999
MODIFICATION OF JMS NEEDLES AND JMS SYRINGES
General Hospital
88d
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