Medical Device Recalls
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1 result found
510(K) Number: K991598 |
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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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Acetaminophen Test System for use on the COBAS/INTEGRA/cobas c, part number 20767174322, Roche Dia... | 2 | 03/16/2011 | Roche Diagnostics Operations, Inc. |
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