Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K201725 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Philips DigitalDiagnost C50 -intended for use in generating radiographic images of human anatomy Mo... | 2 | 04/12/2023 | Philips North America Llc |
DigitalDiagnost C50 1.1-intended for use in generating radiographic images of human anatomy Model N... | 2 | 04/12/2023 | Philips North America Llc |
DigitalDiagnost C50 1.1 | 2 | 09/01/2022 | Philips North America Llc |
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