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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 4 of 4 Results
510(K) Number: K032369
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FDA Recall
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ApexPro Telemetry System - Product Usage: The ApexPro Telemetry System is intended for use under the... 2 12/20/2019 GE Healthcare, LLC
ApexPro Telemetry Server System. Also identified as Modification To: ApexPro Telemetry System and A... 2 10/23/2019 GE Healthcare, LLC
GE Healthcare ApexPro Telemetry System for mobile patient physiological monitoring. 2 06/01/2009 GE Healthcare
GE ApexPro CH Telemetry System. The ApexPro Telemetry System is composed of 6 major components. -T... 2 10/20/2006 Ge Healthcare
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