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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 2 of 2 Results
510(K) Number: K073051
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Recall
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FDA Recall
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Medrad Continuum MR Infusion system- non-wireless system The MEDRAD Continuum MR Infusion System ... 2 05/30/2014 Bayer Corp
Medrad(R) Continuum MR Infusion Pump Peristaltic Pump System designed for patients who require me... 2 12/20/2012 Medrad Inc
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