FDA 510(k) Applications Submitted by LEVITRONIX LLC.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K020271	01/28/2002	LEVITRONIX CENTRIMAG EXTRACORPOREAL BLOOD PUMPING SYSTEM, MODEL L-100	LEVITRONIX LLC.
K051209	05/11/2005	LEVITRONIX CENTRIMAG BACK-UP CONSOLE	LEVITRONIX LLC.
K102129	07/29/2010	LEVITRONIX 2ND GENERATION CENTRIMAG PRIMARY CONSOLE, LEVITRONIX MONITOR	LEVITRONIX LLC.
K053630	12/29/2005	LEVITRONIX CENTRIMAG PRIMARY CONSOLE	LEVITRONIX LLC.
K110980	04/07/2011	CENTRIMAG RETURN CANNULA KIT	LEVITRONIX LLC.
K090004	01/02/2009	LEVITRONIX, THORATEC CENTRIMAG BACK-UP CONSOLES	LEVITRONIX LLC.
K090051	01/07/2009	LEVITRONIX PEDIMAG BLOOD PUMP, MODEL 201-90052	LEVITRONIX LLC.
K081221	04/30/2008	LEVITRONIX CENTRIMAG PRIMARY CONSOLE, THORATEC CENTRIMAG PRIMARY CONSOLE	LEVITRONIX LLC.
K083340	11/12/2008	LEVITRONIX CENTRIMAG PRIMARY CONSOLE; THORATEC CANTRIMAG PRIMARY CONSOLE	LEVITRONIX LLC.
K093832	12/14/2009	LEVITRONIX CENTRIMAG PRIMARY AND BACKUP CONSOLES	LEVITRONIX LLC.