Medical Device Recalls
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1 result found
510(K) Number: K083111 |
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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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| Impella 5.0 Circulatory Support System Catalog number: 004840 The Impella 5.0 System is intended f... | 2 | 09/07/2010 |
FEI # 1220648 Abiomed, Inc. |
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