Medical Device Recalls
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1 result found
510(K) Number: K121213 |
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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 Brain Perfusion made available in various configurations under the names Vitrea, Vitrea f... | 2 | 04/26/2013 | Vital Images, Inc. |
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