Medical Device Recalls
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1 result found
510(K) Number: K152785 |
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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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Angio WorkStation (XIDF-AWS801) used in conjunction with your Infinix System (INFX-8000V;INFX-8000C;... | 2 | 05/30/2017 | Toshiba American Medical Systems Inc |
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