Medical Device Recalls
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1 result found
510(K) Number: K121762 |
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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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GE Healthcare, CardiacVX [CardiacVX (1.1.0 Ext. d) and CardiacVX Flow (1.1.0 Ext. d) analysis softwa... | 2 | 04/25/2014 | GE Healthcare, LLC |
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