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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K130849
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IntelliVue Patient Monitor MX400. Product Number: 866060. 2 12/02/2025 FEI # 3016618143
Philips North America Llc
IntelliVue Patient Monitor MX450. Product Number: 866062. 2 12/02/2025 FEI # 3016618143
Philips North America Llc
IntelliVue Patient Monitor MX550 with L.x and M.x; K.x provided with L.x entitlements Model Number:... 2 08/05/2024 FEI # 3016618143
Philips North America Llc
IntelliVue Patient Monitor MX450 with L.x and M.x; K.x provided with L.x entitlements Model Number... 2 08/05/2024 FEI # 3016618143
Philips North America Llc
IntelliVue Patient Monitor MX400 with L.x and M.x; K.x provided with L.x entitlements Model Number:... 2 08/05/2024 FEI # 3016618143
Philips North America Llc
IntelliVue Patient Monitor MX500 with L.x and M.x; K.x provided with L.x entitlements Model Number:... 2 08/05/2024 FEI # 3016618143
Philips North America Llc
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