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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 8 of 8 Results
510(K) Number: K810352
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Product Description
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FDA Recall
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Edwards Lifesciences Swan-Ganz Thermodilution VIP Catheters Model 131F7J. For use in patients who... 2 08/12/2012 Edwards Lifesciences, LLC
Edwards Lifesciences Swan-Ganz Thermodilution VIP Catheters Model 131F7P. For use in patients who... 2 08/12/2012 Edwards Lifesciences, LLC
Edwards Lifesciences Swan-Ganz Thermodilution VIP Catheters Model 131HF7J. For use in patients wh... 2 08/12/2012 Edwards Lifesciences, LLC
Edwards Lifesciences Swan-Ganz Thermodilution VIP Catheters Model TS057HF7. For use in patients w... 2 08/12/2012 Edwards Lifesciences, LLC
Edwards Lifesciences Swan-Ganz Thermodilution VIP Catheters Model 131HVF7P. For use in patients w... 2 08/12/2012 Edwards Lifesciences, LLC
Edwards Lifesciences Swan-Ganz Thermodilution VIP Catheters Model 151F7. For use in patients who ... 2 08/12/2012 Edwards Lifesciences, LLC
Edwards Lifesciences Swan-Ganz Thermodilution VIP Catheters Model 151HF7. For use in patients who... 2 08/12/2012 Edwards Lifesciences, LLC
Edwards Lifesciences Swan-Ganz Thermodilution VIP Catheters Model 131HF7P. For use in patients wh... 2 08/12/2012 Edwards Lifesciences, LLC
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