Medical Device Recalls
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1 result found
510(K) Number: K940795 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Swan-Ganz CCO/Sv02/CEDV/VIP Thermodilution Catheters model number 744HF75. Flow-directed pulmonary ... | 2 | 06/02/2015 |
FEI # 2015691 Edwards Lifesciences, LLC |
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