Medical Device Recalls
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1 result found
510(K) Number: K092463 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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B-Care 5, Catalog 25-60-00, for use with Sorin HLM C5 and HLM S5. | 2 | 07/22/2010 | Sorin Group USA, Inc. |
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