Medical Device Recalls
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1 result found
510(K) Number: K093279 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Xlumena brand NAVIX Access Device, Model/Catalogue Number: NVX-10-03, Part Number: FG-00666, Product... | 2 | 09/09/2013 | Xlumena, Inc. |
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