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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 8 of 8 Results
510(K) Number: K101571
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Philips Xper Flex Cardio (FC2010, Procedure Room and FC2020, Bedside Monitor) devices - intended for... 2 04/29/2021 Philips North America Llc
Xper Flex Cardio Physiomonitoring System, Software versions 1.5.16.0322 and 1.6.1.0390, Model Number... 2 12/14/2018 Philips Electronics North America Corporation
Xper Flex Cardio Physiomonitoring System, Software version 1.6.0.0388 2 11/14/2018 Invivo Corporation
Xper Flex Cardio Physiomonitoring System Model # 453564669081 Software Version 1.6.0.0388 2 09/18/2018 Invivo Corporation
Xper Flex Cardio Physiomonitoring System The Xper Flex Cardio physiomonitoring system is used to ... 2 06/07/2018 Invivo Corporation
Xper Flex Cardio Physiomonitoring system. Used to facilitate invasive investigations of heart and... 2 12/19/2017 Invivo Corporation
Xper Flex Cardio PhysioMonitoring system The Xper Flex Cardio physiomonitoring system is used to f... 2 11/09/2017 Invivo Corporation
The system provides the ability to transmit patient data files for storage, viewing and analysis at ... 2 09/08/2016 Invivo Corporation
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