Medical Device Recalls
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1 result found
510(K) Number: K113181 |
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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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CellTracks Analyzer II. A semi-automated fluorescence microscope used to enumerate fluorescently ... | 2 | 02/13/2012 | Veridex, LLC |
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