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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 7 of 7 Results
510(K) Number: K173433
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ProxiDiagnost N90 R.1.0 2 05/15/2023 Philips North America
Philips ProxiDiagnost N90 1.0 (Model 706100) and ProxiDiagnost N90 1.1 (Model 706110)- A multi-func... 2 04/28/2023 Philips North America Llc
ProxiDiagnost R90 1.0 and 1.1 multi-functional general R/F system, Model Numbers 706100 and 706110 2 04/10/2023 Philips North America Llc
ProxiDiagnost N90 is multi-functional general R/F systems. 2 11/24/2021 Philips Healthcare
ProxiDiagnost N90 Image-intensified fluoroscopic x-ray system 2 01/28/2021 PHILIPS HOME HEALTHCARE SOLUTION
ProxiDiagnost N90 2 09/30/2020 Philips North America, LLC
ProxiDiagnost N90, UDI 706100 2 06/03/2020 Philips North America, LLC
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