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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: K212837
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ProxiDiagnost N90- A Multi-functional general Radiography and Fluoroscopy (R/F) system Ref: (1)70610... 2 02/09/2024 FEI # 3006648320
Philips North America
ProxiDiagnost upgrade- A Multi-functional general Radiography and Fluoroscopy (R/F) system Ref:7061... 2 02/09/2024 FEI # 3006648320
Philips North America
ProxiDiagnost N90, Radiography and Fluoroscopy (R/F) system 2 11/08/2023 FEI # 3016618143
Philips North America Llc
ProxiDiagnost N90. radiography and fluoroscopy system 2 07/12/2022 FEI # 3003768251
Philips Medical Systems DMC GmbH
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