Medical Device Recalls
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1 result found
510(K) Number: K061974 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| GEM Premier 4000 Laboratory Analyzer | 2 | 05/03/2007 |
FEI # 1217183 Instrumentation Laboratory Co. |
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