Levitronix, LLC
Levitronix, LLC holds FDA 510(k) medical device clearances, first cleared 2003, most recent 2011.
Top product codes for Levitronix, LLC
Recent clearances by Levitronix, LLC
- K110980 — CENTRIMAG RETURN CANNULA KIT
- K110983 — CENTRIMAG DRAINAGE CANNULA KIT
- K102129 — LEVITRONIX 2ND GENERATION CENTRIMAG PRIMARY CONSOLE, LEVITRONIX MONITOR
- K093832 — LEVITRONIX CENTRIMAG PRIMARY AND BACKUP CONSOLES
- K090051 — LEVITRONIX PEDIMAG BLOOD PUMP, MODEL 201-90052
- K090004 — LEVITRONIX, THORATEC CENTRIMAG BACK-UP CONSOLES
- K083340 — LEVITRONIX CENTRIMAG PRIMARY CONSOLE; THORATEC CANTRIMAG PRIMARY CONSOLE
- K081221 — LEVITRONIX CENTRIMAG PRIMARY CONSOLE, THORATEC CENTRIMAG PRIMARY CONSOLE
- K053630 — LEVITRONIX CENTRIMAG PRIMARY CONSOLE
- K051209 — LEVITRONIX CENTRIMAG BACK-UP CONSOLE
- K020271 — LEVITRONIX CENTRIMAG EXTRACORPOREAL BLOOD PUMPING SYSTEM, MODEL L-100
Data sourced from openFDA. This site is unofficial and independent of the FDA.