Medical Device Recalls
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1 result found
510(K) Number: K972503 |
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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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Coronary Artery Perfusion Cannula with Balloon (part number CP-2200X). The Coronary Artery Perfusion... | 2 | 09/08/2016 | Sorin Group USA, Inc. |
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