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FDA 510(k) Applications Submitted by JMS North America Corporation
FDA 510(k) Number
Submission Date
Device Name
Applicant
K111948
07/08/2011
WINGEATER V2
JMS NORTH AMERICA CORPORATION
K110157
01/19/2011
SYSLOC MINI V3
JMS NORTH AMERICA CORPORATION
K112178
07/28/2011
JMS APHERESIS NEEDLE SET WINGEATER(R) V2
JMS NORTH AMERICA CORPORATION
K151017
04/16/2015
JMS Harmony A.V. Fistula Needle Set
JMS NORTH AMERICA CORPORATION
K132321
07/25/2013
JMS SYRINGE
JMS NORTH AMERICA CORPORATION
K172499
08/18/2017
NEOSHIELD
JMS North America Corporation
K142564
09/11/2014
JMS SysLoc MINI A.V. Fistula Needle Set (V4), JMS SysLoc MINI Apheresis Needle Set (V4)
JMS North America Corporation
K121488
05/18/2012
JMS SAFE WING CATH (SWC)
JMS NORTH AMERICA CORPORATION
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