Medical Device Recalls
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1 result found
510(K) Number: K091498 |
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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 5.1. Vitrea fX 3.0, Vitrea Enterprise Suite 1.2 with the licensing of CT lung or CT Colon. | 2 | 05/13/2010 | Vital Images, Inc. |
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