Medical Device Recalls
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1 result found
510(K) Number: K990705 |
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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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Coaxial Micro-Introducer Kit. Greatbatch Part Number/Bard Access Systems Order Number/Part Descri... | 2 | 05/13/2014 | Greatbatch Medical |
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