Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K032458 |
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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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Architect FSH Calibrators (LN 6C24-01), for in vitro diagnostic use. | 2 | 10/12/2006 | Abbott Diagnostic International, Ltd. |
FSH Calibrators (LN 9C06-01), for in vitro diagnostic use. | 2 | 10/12/2006 | Abbott Diagnostic International, Ltd. |
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