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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 10 of 10 Results
510(K) Number: K131497
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Change Healthcare Cardiology Hemo Software 2 07/02/2025 FEI # 3003757840
CHANGE HEALTHCARE CANADA COMPANY
McKesson Cardiology Hemo software 2 01/16/2025 FEI # 3394
A L I Technologies Ltd
Change Healthcare Cardiology Hemo software 2 01/16/2025 FEI # 3394
A L I Technologies Ltd
Change Healthcare Cardiology Hemo. Versions 14.2, 14.1.1, 14.2, 14.3, 14.3.2, 14.3, 15.0.1, 15.1. ... 2 10/17/2024 FEI # 3003757840
CHANGE HEALTHCARE CANADA COMPANY
McKesson Cardiology Hemo. Versions 13.0, 13.1.1, 13.1.2, 13.2, 13.2.1, 14.0. 2 10/17/2024 FEI # 3003757840
CHANGE HEALTHCARE CANADA COMPANY
Horizon Cardiology Hemo 2 05/24/2019 FEI # 3007784465
Change Healthcare Israel Ltd.
McKesson Cardiology Hemo 2 05/24/2019 FEI # 3007784465
Change Healthcare Israel Ltd.
McKesson Cardiology Hemo, Release SW version 13.0. Used for physiological monitoring, image and dat... 2 08/31/2018 FEI # 3007784465
McKesson Israel Ltd.
McKesson Cardiology Hemo. McKesson Cardiology" Hemo is intended for complete physiological/hemody... 2 10/20/2014 FEI # 3002684279
Mckesson Information Solutions LLC
McKesson Cardiology" Hemo intended for complete physiological/hemodynamic monitoring, clinical data ... 2 10/08/2014 FEI # 3002684279
Mckesson Information Solutions LLC
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