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U.S. Department of Health and Human Services

Medical Device Recalls
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21 to 22 of 22 Results
510(K) Number: K063144
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VITROS&amp;amp;amp;amp;reg; 5,1 FS System, Product Codes: 6801375 &amp;amp;amp;amp;amp; 680... 2 04/26/2012 FEI # 1000305841
Ortho-Clinical Diagnostics
enGen(TM) Laboratory Automation Systems configured with Hettich Rotanta 46 RSC Robotic Centrifuges, ... 2 01/26/2012 FEI # 1000136573
Ortho-Clinical Diagnostics
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