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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K061597
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Product Description
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Recall
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FDA Recall
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Recalling Firm
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epoc Host 2 as follows: Product SMN epoc Host 10736387 epoc Host 2, Canada 1073... 2 03/03/2023 FEI # 3002637618
Siemens Healthcare Diagnostics Inc
EPOC BGE Test Card The EPOC Blood Analysis System is intended for use by trained medical professi... 2 02/06/2009 FEI # 3004959793
Epocal
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