Medical Device Recalls
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1 result found
510(K) Number: K071331 |
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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 (available in various configuration as Vitrea Enterprise Suite). Vitrea Enterprise Suite 1.2,... | 2 | 01/11/2012 | Vital Images, Inc. |
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