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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: K183101
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Zenition 50; Product Number (REF): 718096; Interventional fluoroscopic x-ray system 2 10/23/2025 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Zenition 50. Product Code 718096. The devices are used for radiological guidance and visualization ... 2 04/21/2025 FEI # 3016618143
Philips North America Llc
Philips Zenition 50, Model Number: 718096 2 11/12/2024 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Zenition 50 & 70 Mobile Surgery C-arm 2 09/30/2024 FEI # 3006648320
Philips North America
Zenition 50, Model #718096 2 02/17/2022 FEI # 3002807880
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips Zenition 50, System code 718096 - Product Usage: The devices are used for radiological guida... 2 05/08/2020 FEI # 1218950
Philips North America, LLC
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