Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K133972 |
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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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ASPIRE Cristalle (FDR MS-3500) Mammography machine The Fujifilm Digital Mammography Systems, Asp... | 2 | 01/17/2018 | Fujifilm Medical Systems U.S.A., Inc. |
ASPIRE Cristalle (for FDR-3000AWS) The Fujifilm Digital Mammography System, ASPIRE Cristalle (FD... | 2 | 02/20/2018 | Fujifilm Medical Systems U.S.A., Inc. |
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