Medical Device Recalls
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1 result found
510(K) Number: K885281 |
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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 Lifesciences "VAMP Jr" (Venous Arterial blood Management Protection system), Lot numbers (al... | 2 | 08/25/2009 |
FEI # 3003081151 Edwards Lifesciences AG |
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