Medical Device Recalls
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1 result found
510(K) Number: K871945 |
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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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Microlab AT, part numbers 135001, 135001OOC, 135002, 135003, 135005, 135006, 135006R, 135007, 135008... | 2 | 02/14/2006 | Hamilton Co |
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