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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: K173433
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ProxiDiagnost N90 R.1.0 2 05/15/2023 FEI # 3006648320
Philips North America
Philips ProxiDiagnost N90 1.0 (Model 706100) and ProxiDiagnost N90 1.1 (Model 706110)- A multi-func... 2 04/28/2023 FEI # 3016618143
Philips North America Llc
ProxiDiagnost N90 is multi-functional general R/F systems. 2 11/24/2021 FEI # 1218950
Philips Healthcare
ProxiDiagnost N90 Image-intensified fluoroscopic x-ray system 2 01/28/2021 FEI # 3016860078
PHILIPS HOME HEALTHCARE SOLUTION
ProxiDiagnost N90 2 09/30/2020 FEI # 1218950
Philips North America, LLC
ProxiDiagnost N90, UDI 706100 2 06/03/2020 FEI # 1218950
Philips North America, LLC
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