Medical Device Recalls
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1 result found
510(K) Number: K202478 |
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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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Captivator Single-Use Polypectomy Snares, Captiflex Single-Use Polypectomy Snares. Outer box UP... | 2 | 03/04/2021 | Boston Scientific Corporation |
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