Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K043103 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Vigilance II Monitor Model: VIG2/VIG2E Software: versions 00.51, 00.60, 00.61, 00.62, 00.63, 00.64, ... | 2 | 02/02/2012 | Edwards Lifesciences, Llc |
| Edwards Vigilance II Continuous Cardiac Output/Oximetry/Volumetric (CCO/SvO2/CEDV) Monitor Model: VI... | 2 | 11/24/2007 | Edwards Lifesciences, Llc |
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