Medical Device Recalls
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1 result found
510(K) Number: K060816 |
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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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MIM 4.0 and MIM 4.1 is a software package designed for use in diagnostic imaging. It is a stand alon... | 2 | 09/03/2008 | MIMvista Corp |
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