Medical Device Recalls
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1 result found
510(K) Number: K112114 |
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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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FLOW-I Anesthesia System The system is intended for use in administrating anesthesia while contro... | 1 | 07/06/2012 | Maquet Cardiovascular Us Sales, Llc |
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