Medical Device Recalls
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1 result found
510(K) Number: K162771 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| EKOS Control Unit 4.0 console, a component of the EKOS Control System 4.0, which is a component of t... | 2 | 10/28/2022 | Boston Scientific Corporation |
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