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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
510(K) Number: K132829
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Quadrox-iD Adult Diffusion Membrane Oxygenator Product Usage: The Quadrox-iD Adult Diffusion Mem... 2 05/28/2015 FEI # 3008355164
Maquet Cardiovascular Us Sales, Llc
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