Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K023582 |
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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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i-STAT ACT Kaolin Cartridges in vitro diagnostic test which uses fresh whole blood to monitor high-... | 2 | 11/17/2010 | Abbott Point Of Care Inc. |
Abbott i-STAT ACT Kaolin Cartridges. In vitro diagnostic test which uses fresh whole blood to mon... | 2 | 02/23/2010 | Abbott Point of Care Inc. |
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