Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K090357 |
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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 HydroFrame 18, HydroCoil Embolic System, Endovascular Embolization Coil, Sterile... | 2 | 02/27/2020 | Microvention, Inc. |
MicroVention Terumo HydroFrame 10, HydroCoil Embolic System, Endovascular Embolization Coil, Sterile... | 2 | 02/27/2020 | Microvention, Inc. |
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