Medical Device Recalls
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1 result found
510(K) Number: K110051 |
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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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Cordis a Johnson & Johnson Company, RadialSource Spring Wire Transradial Access Kit. Manufacturer Gr... | 2 | 06/27/2013 | Greatbatch Medical |
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