Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K091641 |
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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 HydroSoft 10, HydroCoil Embolic System, Endovascular Embolization Coil, Helical,... | 2 | 02/27/2020 | Microvention, Inc. |
MicroVention Terumo Microplex 10, Platinum Coil System, Endovascular Embolization Coil, HyperSoft 3D... | 2 | 02/27/2020 | Microvention, Inc. |
MicroVention Terumo Microplex 10, Platinum Coil System, Endovascular Embolization Coil, HyperSoft He... | 2 | 02/27/2020 | Microvention, Inc. |
MicroVention Terumo Microplex 18, Platinum Coil System, Endovascular Embolization Coil, Helical 18 S... | 2 | 02/27/2020 | Microvention, Inc. |
MicroVention Terumo HydroSoft 10, HydroCoil Embolic System, Endovascular Embolization Coil, HydroSof... | 2 | 02/27/2020 | Microvention, Inc. |
MicroVention Terumo Microplex 10, Platinum Coil System, Endovascular Embolization Coil, Helical 10 S... | 2 | 02/27/2020 | Microvention, Inc. |
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