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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K993825
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ADVIA® 120/2120/2120i 3-in-1 TESTpoint Control (ABN1 Control) 2 07/03/2025 FEI # 2432235
Siemens Healthcare Diagnostics, Inc.
ADVIA® 120/2120/2120i 3-in-1 TESTpoint Control (ABN2 Control) 2 07/03/2025 FEI # 2432235
Siemens Healthcare Diagnostics, Inc.
ADVIA® 120/2120/2120i 3-in-1 TESTpoint Control (Norm Control) 2 07/03/2025 FEI # 2432235
Siemens Healthcare Diagnostics, Inc.
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