Medical Device Recalls
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1 result found
510(K) Number: K111900 |
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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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The Arrow Edge Hemodialysis Catheterization Set Long-Term Access and NextStep Antegrade Hemodialysis... | 2 | 01/22/2015 | Arrow International Inc |
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