Medical Device Recalls
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1 result found
510(K) Number: K042243 |
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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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Microalbumin Multi-Calibrator Set, in vitro diagnostic. Catalog Number: SE-252 | 3 | 02/27/2007 | Diagnostic Chemicals, Ltd. |
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