Medical Device Recalls
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1 result found
510(K) Number: K023354 |
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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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Compressor Mini To provide a supply of dry, filtered compressed air for a medical respiratory ven... | 2 | 01/28/2014 | Maquet Cardiovascular Us Sales, Llc |
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