Today, the @US_FDA is providing an update on our evaluation of device failure associated with Getinge ' s Maquet/Datascope intra-aortic balloon pump (IABP) devices.pic.twitter.com/6eDYSscIgx

Today, the @US_FDA is providing an update on our evaluation of device failure associated with Getinge's Maquet/Datascope intra-aortic balloon pump (IABP) devices. pic.twitter.com/6eDYSscIgx

https://twitter.com/FDADeviceInfo/status/1196837212693901313

Source: Food and Drug Adminstration (FDA): CDRHNew - November 19, 2019 Category: Medical Devices Authors: ( at FDADeviceInfo) Source Type: news

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