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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: K203087
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CombiDiagnost R90 R1.1 2 05/15/2023 Philips North America
CombiDiagnost R90 1.0 and 1.1 multi-functional general R/F system, Model Numbers 709030 and 709031 2 04/10/2023 Philips North America Llc
CombiDiagnost R90 is multi-functional general R/F systems. 2 11/24/2021 Philips Healthcare
CombiDiagnost R90 Software Version R1.0 and R1.1 2 08/28/2021 Philips Medical Systems Gmbh, DMC