FDA 510(k) Applications Submitted by JMS NORTH AMERICA CORP.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K070143	01/16/2007	JMS PLANECTA STOPCOCK	JMS NORTH AMERICA CORP.
K040247	02/03/2004	PLUME SAFETY AVF NEEDLE	JMS NORTH AMERICA CORP.
K051814	07/05/2005	JMS SYSLOC MINI A.V. FISTULA NEEDLE SET AND APHERESIS NEEDLE SET	JMS NORTH AMERICA CORP.
K093637	11/24/2009	JMS BLUNT A. V. FISTULA NEEDLE SET WITH SITE PREPARATION TOOL MODEL 820-5300, 820-6300 AND 820-7300	JMS NORTH AMERICA CORP.
K082882	09/30/2008	A.V. FISTULA BLUNT NEEDLE SET	JMS NORTH AMERICA CORP.
K030479	02/13/2003	JMS SYSLOC A.V. FISTULA NEEDLE SET, JMS SYSLOC APHERESIS NEEDLE SET	JMS NORTH AMERICA CORP.
K032975	09/24/2003	JMS BLOOD TUBING SETS	JMS NORTH AMERICA CORP.
K070234	01/16/2007	JMS SYSLOC MINI AVF AND APHERESIS NEEDLE SETS	JMS NORTH AMERICA CORP.
K032977	09/24/2003	JMS BYPASS TUBE	JMS NORTH AMERICA CORP.
K023668	10/31/2002	JMS EXTENSION SET WITH PLANECTA, PLANECTA (STAND ALONE UNIT), PLANECTA LOCK & PLANECTA ADAPTOR	JMS NORTH AMERICA CORP.