Levitronix, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Levitronix, LLC - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Levitronix, LLC has 11 FDA 510(k) cleared cardiovascular devices. Based in Waltham, US.
Historical record: 11 cleared submissions from 2003 to 2011.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Levitronix, LLC
11 devices
Cleared
Jun 20, 2011
CENTRIMAG RETURN CANNULA KIT
Cardiovascular
74d
Cleared
Jun 20, 2011
CENTRIMAG DRAINAGE CANNULA KIT
Cardiovascular
74d
Cleared
Aug 27, 2010
LEVITRONIX 2ND GENERATION CENTRIMAG PRIMARY CONSOLE, LEVITRONIX MONITOR
Cardiovascular
29d
Cleared
Jan 13, 2010
LEVITRONIX CENTRIMAG PRIMARY AND BACKUP CONSOLES
Cardiovascular
30d
Cleared
Oct 08, 2009
LEVITRONIX PEDIMAG BLOOD PUMP, MODEL 201-90052
Cardiovascular
274d
Cleared
Jan 15, 2009
LEVITRONIX, THORATEC CENTRIMAG BACK-UP CONSOLES
Cardiovascular
13d
Cleared
Nov 26, 2008
LEVITRONIX CENTRIMAG PRIMARY CONSOLE
Cardiovascular
14d
Cleared
Jun 19, 2008
LEVITRONIX CENTRIMAG PRIMARY CONSOLE, THORATEC CENTRIMAG PRIMARY CONSOLE
Cardiovascular
50d
Cleared
Jan 26, 2006
LEVITRONIX CENTRIMAG PRIMARY CONSOLE
Cardiovascular
28d
Cleared
Sep 08, 2005
LEVITRONIX CENTRIMAG BACK-UP CONSOLE
Cardiovascular
120d
Cleared
Mar 25, 2003
LEVITRONIX CENTRIMAG EXTRACORPOREAL BLOOD PUMPING SYSTEM, MODEL L-100
Cardiovascular
421d