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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: K131872
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IntelliVue Patient Monitor MX400 (Model Number 866060), MX430 (Model Number 866061), MX450 (Model Nu... 2 09/25/2024 FEI # 3006648320
Philips North America
IntelliVue Patient Monitor MX550. Product Number: 866066. 2 12/02/2025 FEI # 3016618143
Philips North America Llc
IntelliVue Patient Monitor MX500. Product Number: 866064. 2 12/02/2025 FEI # 3016618143
Philips North America Llc
IntelliVue Patient Monitor MX400/MX450/MX500/MX550 with software version P.01.01 and ordered with Op... 2 10/04/2024 FEI # 3016618143
Philips North America Llc
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