Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K190401 |
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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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MAMBA Microcatheter. Packaged with protective sleeve over catheter, sealed in a Tyvek pouch, and is... | 2 | 04/15/2021 | Boston Scientific Corporation |
MAMBA Flex 135 Microcatheter. Packaged with protective sleeve over catheter, sealed in a Tyvek pouc... | 2 | 04/15/2021 | Boston Scientific Corporation |
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