Medical Device Recalls
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1 result found
510(K) Number: K121916 |
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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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Aquarius iNtuition Client Viewer. Findings Workflow module, RECIST 1.1: Picture Archiving and Commu... | 2 | 02/09/2015 | TeraRecon, Inc. |
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