Medical Device Recalls
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1 result found
510(K) Number: K933212 |
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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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IMMULITE Systems Rapid TSH (REF LKRT1 - 100T, LKRT5 - 500 T, L2KRT2 - 200T, L2KRT6 - 600T). Inten... | 2 | 08/06/2013 | Siemens Healthcare Diagnostics, Inc |
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