Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K051052 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| IceRod" 1.5 Cryoablation Needle | 2 | 12/22/2020 |
FEI # 3002095335 Boston Scientific Corporation |
| IceRod" 1.5 MRI 90® Cryoablation Needle® | 2 | 12/22/2020 |
FEI # 3002095335 Boston Scientific Corporation |
| IceRod" Prostate Cryoablation Kit | 2 | 12/22/2020 |
FEI # 3002095335 Boston Scientific Corporation |
| IceSeed" 1.5® MRI 90® Cryoablation Needle ® | 2 | 12/22/2020 |
FEI # 3002095335 Boston Scientific Corporation |
| IceSeed" 1.5 MRI Cryoablation Needle | 2 | 12/22/2020 |
FEI # 3002095335 Boston Scientific Corporation |
| IceRod" 1.5 MRI Cryoablation Needle® | 2 | 12/22/2020 |
FEI # 3002095335 Boston Scientific Corporation |
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