Medical Device Recalls
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1 result found
510(K) Number: K021641 |
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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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| The D*Clot® HD Rotational Thrombectomy System is a percutaneous catheter-based system available in 6... | 2 | 06/26/2024 |
FEI # 3007146453 Mermaid Medical A/S |
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