Medical Device Recalls
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1 result found
510(K) Number: K110012 |
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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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illumipro-10 Incubator/Reader, Meridian Bioscience, Inc. The illumipro-10 incubator/reader is des... | 2 | 06/27/2014 | Meridian Bioscience Inc |
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