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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K160944
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Accu-Chek Guide (SC) Kit -Intended to quantitatively measure glucose in fresh capillary whole blood ... 2 06/21/2024 FEI # 3011393376
Roche Diabetes Care, Inc.
Blood Glucose Monitoring System, Model Number 07400870001 ACCU-CHEK GUIDE SAMPLE KIT MG/DL - Produc... 2 12/30/2019 FEI # 3011393376
Roche Diabetes Care, Inc.
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