Medical Device Recalls
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1 result found
510(K) Number: K162901 |
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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 3D Revascularization Device It is indicated for used in the revascularization of patients ... | 1 | 06/22/2017 | Penumbra Inc. |
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