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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 7 of 7 Results
510(K) Number: K102495
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FDA Recall
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Intellivue iX Information Center Software - All PIIC iX Surveillance stations including: 866023 Int... 2 02/28/2018 Philips Electronics North America Corporation
Philips Healthcare IntelliVue Info Center iX, A.0 866023 2 02/23/2016 Philips Electronics North America Corporation
Philips Healthcare IntelliVue Info Center iX, B.0, 866389 Physiological, Patient Monitor (With Ar... 2 02/23/2016 Philips Electronics North America Corporation
Philips Healthcare PIIC Classic Upgrade, 866117 Physiological, Patient Monitor (With Arrhythmia De... 2 02/23/2016 Philips Electronics North America Corporation
Philips IntelliVue Information Center iX (release A.00, A.01, and A.02) are impacted by this issue: ... 2 12/04/2015 Philips Medical Systems, Inc.
Philips IntellVue Info Center iX 866023; PIIC iX Upgrade 866024; IntellVue Server iX Upgrade 866026;... 2 06/11/2014 Philips Healthcare Inc.
Philips IntelliVue Information Center/Client and Philips IntelliVue Information Center iX The in... 2 12/10/2012 Philips Healthcare Inc.
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