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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K962126
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ADVIA Centaur CKMB Calibrator 2-pack Japan, Cat No. 02562748 Product Usage: For in vitro diagnos... 2 10/15/2018 FEI # 1219913
Siemens Healthcare Diagnostics, Inc
ADVIA Centaur CKMB Calibrator, Cat No. 09318028 Product Usage: For in vitro diagnostic use in ca... 2 10/15/2018 FEI # 1219913
Siemens Healthcare Diagnostics, Inc
ADVIA Centaur CKMB Master Curve Material, Cat No. 07867768 Product Usage: For in vitro diagnos... 2 10/15/2018 FEI # 1219913
Siemens Healthcare Diagnostics, Inc
Atellica IM CKMB Calibrator, Cat No. 10995532 Product Usage: For in vitro diagnostic use for e... 2 10/15/2018 FEI # 1219913
Siemens Healthcare Diagnostics, Inc
Atellica IM CKMB Master Curve Material, Cat No. 10995534 Product Usage: For in vitro diagnosti... 2 10/15/2018 FEI # 1219913
Siemens Healthcare Diagnostics, Inc
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