Medical Device Recalls
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1 result found
510(K) Number: K090147 |
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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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Blood Monitoring Unit (BMU 40), model no. 701040852 - Product Usage: is to monitor blood parameters ... | 2 | 11/12/2020 | Maquet Cardiovascular Us Sales, Llc |
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