Medical Device Recalls
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1 result found
510(K) Number: K043333 |
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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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Vitrea CT Multi-Chamber Cardiac Functional Analysis application on Vitrea version 5.2 (Vitrea Enterp... | 2 | 04/18/2013 | Vital Images, Inc. |
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