Medical Device Recalls
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1 result found
510(K) Number: K902628 |
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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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| EDWARDS VIGILANCE MONITORS (FORMERLY BAXTER VIGILANCE MONITORS) with software release 5.3 or earli... | 2 | 08/02/2006 |
FEI # 2015691 Edwards Lifesciences Llc |
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