Medical Device Recalls
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1 result found
510(K) Number: K161452 |
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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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MicroVention Terumo Microplex 10, Platinum Coil System, Endovascular Embolization Coil, HyperSoft 3D... | 2 | 02/27/2020 | Microvention, Inc. |
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