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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K100433
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IMMULITE 2000/IMMULITE 2000XPi Systems CMM CMV IgM Assay, REF/Catalog Number L2KCM2(D) - 200 tests (... 2 10/27/2016 FEI # 2432235
Siemens Healthcare Diagnostics, Inc.
IMMULITE/ IMMULITE 1000 Systems CMM CMV IgM Assay, REF/Catalog Number LKCM1(D) - 100 tests (US), Sie... 2 10/27/2016 FEI # 2432235
Siemens Healthcare Diagnostics, Inc.
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