Medical Device Recalls
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1 result found
510(K) Number: K022880 |
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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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Maquet Heartstring II Proximal Seal System (HS-1045) manufactured by Maquet Cardiovascular, Wayne, N... | 1 | 02/01/2011 | Maquet Cardiovascular, LLC |
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