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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: K163410
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Philips DigitalDiagnost C50 -intended for use in generating radiographic images of human anatomy Mo... 2 04/12/2023 FEI # 3016618143
Philips North America Llc
DigitalDiagnost C50, Stationary X-ray System 2 09/20/2019 FEI # 1218950
Philips Healthcare
DigitalDiagnost C50 1.1-intended for use in generating radiographic images of human anatomy Model N... 2 04/12/2023 FEI # 3016618143
Philips North America Llc
DigitalDiagnost C50 1.1 2 09/01/2022 FEI # 3016618143
Philips North America Llc
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