Jms North America Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Jms North America Corp. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Jms North America Corp. has 10 FDA 510(k) cleared medical devices. Based in Hayward, US.
Historical record: 10 cleared submissions from 2003 to 2010. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Jms North America Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Jms North America Corp.
10 devices
Cleared
Feb 09, 2010
JMS BLUNT A. V. FISTULA NEEDLE SET WITH SITE PREPARATION TOOL MODEL 820-5300,...
Gastroenterology & Urology
77d
Cleared
Jan 21, 2009
A.V. FISTULA BLUNT NEEDLE SET
Gastroenterology & Urology
113d
Cleared
May 22, 2007
JMS SYSLOC MINI AVF AND APHERESIS NEEDLE SETS
Gastroenterology & Urology
126d
Cleared
Apr 10, 2007
JMS PLANECTA STOPCOCK
General Hospital
84d
Cleared
Aug 04, 2005
JMS SYSLOC MINI A.V. FISTULA NEEDLE SET AND APHERESIS NEEDLE SET
Gastroenterology & Urology
30d
Cleared
Aug 16, 2004
JMS BLOOD TUBING SETS
Gastroenterology & Urology
327d
Cleared
May 25, 2004
JMS BYPASS TUBE
Cardiovascular
244d
Cleared
Mar 03, 2004
PLUME SAFETY AVF NEEDLE
Gastroenterology & Urology
29d
Cleared
Aug 18, 2003
JMS SYSLOC A.V. FISTULA NEEDLE SET, JMS SYSLOC APHERESIS NEEDLE SET
General Hospital
186d
Cleared
Jul 01, 2003
JMS EXTENSION SET WITH PLANECTA, PLANECTA (STAND ALONE UNIT), PLANECTA LOCK &...
General Hospital
243d