Jms North America Corp. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
FDA 510(k) Regulatory Record - Jms North America Corp. Gastroenterology & Urology ✕
6 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
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
Mar 03, 2004
PLUME SAFETY AVF NEEDLE
Gastroenterology & Urology
29d