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aortic balloon pump

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aortic balloon pump.


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1999) Intra aortic balloon pump (IABP) counterpulsation [Web document].
Food and Drug Administration (FDA) has classified the voluntary medical device recall initiated on February 2, 2009 by Arrow International's Cardiac Care Division involving volume connectors for its 30cc, 40cc and 50cc Intra Aortic Balloon Pump (IAB) Catheters as a Class 1 recall.
Nasdaq:DSCP) announced today that the companies have entered into a definitive distribution agreement for Datascope's Intra Aortic Balloon Pumps (IABP) and Intra Aortic Balloon (IAB) catheters in Japan.
 
 
 
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