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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K060548
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Siemens Acute Care BHCG CalPak-in vitro diagnostic product intended to be used for calibration of th... 2 01/07/2016 FEI # 3002637618
Siemens Healthcare Diagnostics Inc
Siemens Acute Care BHCG TestPak-an in vitro diagnostic product intended to be used for calibration o... 2 01/07/2016 FEI # 3002637618
Siemens Healthcare Diagnostics Inc
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