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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K031393
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Recall
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ADVIA Centaur CA 19-9 Assay (50 test kit)-for use, with the ADVIA Centaur and ADVIA Centaur XP, ADV... 2 11/17/2016 Siemens Healthcare Diagnostics, Inc
ADVIA Centaur CA 19-9 Assay (250 test kit)-for use,with the ADVIA Centaur and ADVIA Centaur XP, ADV... 2 11/17/2016 Siemens Healthcare Diagnostics, Inc
Siemens Healthcare ADVIA Centaur CA 19-9 250 Test 10491244 50 Test 10491379 Intended Use The A... 2 12/11/2012 Siemens Healthcare Diagnostics, Inc
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