Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K133958 |
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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 Product Usage: The indication for the Flow-i Anesthesia System is admin... | 1 | 02/22/2016 | Maquet Cardiovascular Us Sales, Llc |
The FLOW-i Anesthesia System Axillary O2 and Suction Module, Device Part number: 66 79 847 FLOW-i ... | 2 | 07/15/2015 | Maquet Cardiovascular Us Sales, Llc |
FLOW-i Anesthesia System The FLOW-i Anesthesia System is intended for use administering inhalatio... | 1 | 06/08/2015 | Maquet Cardiovascular Us Sales, Llc |
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