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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: K203087
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CombiDiagnost R90, Radiography and Fluoroscopy (R/F) system 2 11/08/2023 FEI # 3016618143
Philips North America Llc
CombiDiagnost R90 R1.1 2 05/15/2023 FEI # 3006648320
Philips North America
CombiDiagnost R90 Software Version R1.0 and R1.1 2 08/28/2021 FEI # 3003768251
Philips Medical Systems Gmbh, DMC
CombiDiagnost R90 1.1 (709031) 2 02/14/2024 FEI # 3017726341
PHILIPS MEDICAL SYSTEMS
CombiDiagnost R90 is multi-functional general R/F systems. 2 11/24/2021 FEI # 1218950
Philips Healthcare
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