Medical Device Recalls
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1 result found
510(K) Number: K183361 |
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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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| EKOS Control System (CU) 4.0. UPN 600-40500 The EkoSonic MACH4 Endovascular (EKOS) System consi... | 2 | 12/17/2020 |
FEI # 3005099803 Boston Scientific Corporation |
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