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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K082583
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IntelliVue Patient Monitor MX550. Model Number: 866066 2 02/05/2025 FEI # 3016618143
Philips North America Llc
IntelliVue Patient Monitor MX500. Model Number: 866064 2 02/05/2025 FEI # 3016618143
Philips North America Llc
IntelliVue Patient Monitor MX450. Model Number: 866062 2 02/05/2025 FEI # 3016618143
Philips North America Llc
IntelliVue Patient Monitor MX400. Model Number: 866060 2 02/05/2025 FEI # 3016618143
Philips North America Llc
IntelliBridge EC10 Module. Model Number: 865115 2 02/05/2025 FEI # 3016618143
Philips North America Llc
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