Medical Device Recalls
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1 result found
510(K) Number: K101398 |
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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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Software versions Eos software versions: 1.2.4, 1.2.5, 1.2.6,1.2.7,1.2.8, 1.2.9,1.2.10, .2.11,1.2.1... | 2 | 06/28/2011 | Eos Imaging |
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