Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K170858 |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| The device is a mobile x-ray system designed to work with Fujifilm's GOS and CsI scintillator FDR D-... | 2 | 09/25/2024 | FUJIFILM Healthcare Americas Corporation |
| FujiFilm FDR AQRO (Model DR-XD1000)- A digital mobile X-ray system intended for use in general purpo... | 2 | 04/27/2023 | FUJIFILM Healthcare Americas Corporation |
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