Medical Device Recalls
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1 result found
510(K) Number: K993861 |
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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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Genital Protector Shield used with Fuji Computed Radiography (FCR) system models 5501D and XU/D1. M... | 2 | 10/28/2004 | Fujifilm Medical System USA, Inc. |
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