Medical Device Recalls
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1 result found
510(K) Number: K160805 |
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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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NIO-A / NIO-P is an instant IO access device comprises housing with spring load mechanism that injec... | 2 | 08/27/2016 | Waismed Ltd |
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