Medical Device Recalls
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1 result found
510(K) Number: K103305 |
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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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Penumbra brand Penumbra Coil System, Penumbra Coil 400, Product is manufactured and distributed by P... | 1 | 04/12/2011 | Penumbra Inc. |
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