Medical Device Recalls
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1 result found
510(K) Number: K030475 |
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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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| Stryker brand GDC-10 ULTRA SOFT 2MM X 3CM, Catalog Number: M0033432030; Product is manufactured by... | 2 | 12/13/2013 |
FEI # 3008853977 Stryker Neurovascular |
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