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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K123900
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Recall
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FDA Recall
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Philips SureSigns VM4, VM6 and VM8 - Product Usage: patient monitors-for monitoring, recording and a... 2 03/30/2021 Philips North America, LLC
Philips SureSigns VM 3/4/6/8 Patient Monitors, 863063 863064 863065 863066 863068 863077 86308... 2 08/22/2018 Philips Electronics North America Corporation
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